Cyclohexene-3,6-diyl compound, liquid crystal composition and liquid crystal display device

ABSTRACT

To provide a compound, when the compound has both a high clearing point and a low crystallization temperature, having a wide temperature range of a liquid crystal phase and also an excellent solubility in other liquid crystal compounds, and further having general physical properties necessary for the compound, namely, stability to heat, light and so forth, a suitable optical anisotropy and a suitable dielectric anisotropy. A compound is represented by formula (1): 
     
       
         
         
             
             
         
       
     
     wherein, for example, Ra and Rb are alkyl having 1 to 10 carbons; A 1 , A 2 , A 3  and A 4  are 1,4-phenylene; Z 1 , Z 2 , Z 3  and Z 4  are a single bond or alkylene having 1 to 4 carbons; and m, n, q and r are independently 0, 1, or 2, and a sum of m, n, q and r is 1, 2, 3 or 4.

TECHNICAL FIELD

The invention relates to a liquid crystal composition, a liquid crystalcompound and a liquid crystal display device. More specifically, theinvention relates to a cyclohexene-3,6-diyl compound, a liquid crystalcomposition that contains the same and has a nematic phase and a liquidcrystal display device including the composition.

BACKGROUND ART

A liquid crystal display device typified by a liquid crystal displaypanel, a liquid crystal display module and so forth utilizes opticalanisotropy, dielectric anisotropy and so forth of a liquid crystalcompound. As an operating mode of the liquid crystal display device,various kinds of modes are known, such as a phase change (PC) mode, atwisted nematic (TN) mode, a super twisted nematic (STN) mode, abistable twisted nematic (BTN) mode, an electrically controlledbirefringence (ECB) mode, an optically compensated bend (OCB) mode, anin-plane switching (IPS) mode, a vertical alignment (VA) mode and apolymer sustained alignment (PSA) mode.

The liquid crystal display device is required to have capability ofbeing driven in a temperature range from a high temperature to a lowtemperature. However, many cyclohexane rings are used in a compound in acomposition that has been used so far, and compatibility of a compoundhaving such a cyclohexane ring has been poor at a low temperature. Thus,a smectic phase or crystals easily precipitate, and therefore driving ata low temperature has not been easy, in particular. From such abackground, development has been required for a liquid crystal compoundhaving a high clearing point, a low crystallization temperature, anexcellent compatibility and an excellent chemical stability.

For example, compound (A) as described below is reported (Patentliterature No. 1, for example). However, the compound (A) has asignificantly poor liquid crystallinity, and has not been sufficient asa liquid crystal compound constituting a liquid crystal compositionhaving desired physical properties.

Moreover, compound (B) as described below is reported (Non-patentliterature No. 1, for example). However, the compound (B) has a moietyhaving a problem in chemical stability, such as an ester group and acyano group, and has not been sufficient as a liquid crystal compoundconstituting a liquid crystal composition used for a liquid crystaldisplay device in which high reliability is required.

The prior arts are as described below. A further preferred liquidcrystal compound, liquid crystal composition and liquid crystal displaydevice are desired.

CITATION LIST Patent Literature

-   Patent literature No. 1: JP H4-327544 A.

Non-Patent Literature

-   Non-patent literature No. 1: Liq. Cryst., 1989, 4(2), 209-215.

SUMMARY OF INVENTION Technical Problem

A display device that operates according to each mode described above isconstituted of a liquid crystal composition containing a liquid crystalcompound. In order to further improve characteristics of the displaydevice, the liquid crystal compound is required to have characteristicsshown in (1) to (8) below. More specifically, the characteristicsinclude:

(1) being chemically stable and physically stable;(2) having a high clearing point (clearing point: transition temperaturebetween a liquid crystal phase and an isotropic phase);(3) having a low minimum temperature of a liquid crystal phase (anematic phase, a smectic phase or the like), in particular, having a lowminimum temperature of the nematic phase;(4) having a small viscosity;(5) having a suitable optical anisotropy;(6) having a suitable dielectric anisotropy suited for each mode;(7) having a suitable elastic constant suited for each mode; and(8) having an excellent solubility in other liquid crystal compounds.

If a composition containing a liquid crystal compound being chemicallyand physically stable as described in (1) is used for the displaydevice, a voltage holding ratio can be increased. A compositioncontaining a liquid crystal compound having a high clearing point or alow minimum temperature of the liquid crystal phase as described in (2)and (3) allows extension of a temperature range of the nematic phase,and can be used in the form of the display device in a wide temperaturerange.

If a composition containing a compound having a small viscosity asdescribed in (4) and a compound having a suitable elastic constant asdescribed in (7) are used in the form of the display device, responsetime can be improved, and in a case of a display device in which acomposition containing a compound having a suitable optical anisotropyas described in (5) is used, contrast of the display device can beimproved.

In a case where a compound has a suitable dielectric anisotropy suitedfor each mode, a threshold voltage of a liquid crystal compositioncontaining the compound can be decreased, and therefore a drivingvoltage of the display device can be decreased, and electric powerconsumption can also be decreased. Furthermore, when a compositioncontaining a compound having a suitable elastic constant as described in(7) is used in the form of the display device, a driving voltage of thedisplay device can be decreased, and electric power consumption can alsobe decreased.

The liquid crystal compound is generally used in the form of the liquidcrystal composition prepared by mixing the compound with many otherliquid crystal compounds in order to develop characteristics that aredifficult to achieve by a single compound. Accordingly, the liquidcrystal compound to be used for the display device preferably has a goodsolubility in other liquid crystal compounds and so forth as describedin (8). Moreover, because the display device may be occasionally used ina wide temperature range including a freezing point or lower, a compoundhaving a good compatibility at a low temperature is preferred.

A first aim of the invention is to provide a liquid crystal compoundhaving stability to heat, light and so forth, a small viscosity and anexcellent solubility in other liquid crystal compounds, exhibiting anematic phase in a wide temperature range, and having a suitable opticalanisotropy and a suitable elastic constant.

A second aim of the invention is to provide a liquid crystal compositionthat contains the compound, and has a high stability to heat, light andso forth, a low viscosity, a suitable optical anisotropy, a suitabledielectric anisotropy, a suitable elastic constant, a low thresholdvoltage, a high maximum temperature of the nematic phase and a lowminimum temperature of the nematic phase.

A third aim of the invention is to provide a liquid crystal displaydevice that includes the composition, and has a short response time, asmall electric power consumption, a small driving voltage and a largecontrast, and can be used in a wide temperature range.

Solution to Problem

In view of the problems described above, the present inventors havediligently conducted research, as a result, have found that a compoundhaving a double bond on 2-position of a 1,4-cyclohexylene group has botha high clearing point and a low crystallization temperature, and thusthe compound has, while having a wide temperature range of a liquidcrystal phase, an excellent solubility in other liquid crystalcompounds, stability to heat, light and so forth, a small viscosity, asuitable optical anisotropy and a suitable elastic constant, and aliquid crystal composition containing the compound has stability toheat, light and so forth, a small viscosity, a suitable opticalanisotropy, a suitable elastic constant, a suitable dielectricanisotropy, a low threshold voltage, a high maximum temperature of anematic phase and a low minimum temperature of the nematic phase, andfurther a liquid crystal display device including the composition has ashort response time, a small electric power consumption, a small drivingvoltage and a large contrast ratio, and can be used in a widetemperature range, and thus have completed the invention.

The invention includes subject matters described in items 1 to 32 below.Simultaneously, a preferred example of a bonding group in compound (1)will be described.

Item 1. A compound represented by formula (1):

wherein, in formula (1), Ra and Rb are independently hydrogen, halogenor alkyl having 1 to 10 carbons, and in the alkyl, arbitrary —CH₂— maybe replaced by —O—, —S—, —CO— or —SiH₂—, and arbitrary —(CH₂)₂— may bereplaced by —CH═CH— or —C≡C—; A¹, A², A³ and A⁴ are independently1,4-cyclohexylene, 1,4-phenylene, cyclohexene-1,4-diyl,cyclohexene-3,6-diyl, decahydronaphthalene-2,6-diyl,1,2,3,4-tetrahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl, and inthe rings, one of —CH₂— may be replaced by —O—, —S—, —CO— or —SiH₂—, andarbitrary —(CH₂)₂— may be replaced by —CH═CH—, and in the rings,arbitrary hydrogen may be replaced by halogen, —CF₃, —CHF₂, —CH₂F,—OCF₃, —OCHF₂ or —OCH₂F; Z¹, Z², Z³ and Z⁴ are independently a singlebond or alkylene having 1 to 4 carbons, and in the alkylene, arbitrary—CH₂— may be replaced by —O—, —S— or —SiH₂—, and arbitrary —(CH₂)₂— maybe replaced by —CH═CH— or —C≡C—; m, n, q and r are independently 0, 1 or2, and a sum of m, n, q and r is 1, 2, 3 or 4; and when a sum of m, n, qand r is 1, Ra and Rb are independently hydrogen, halogen or alkylhaving 1 to 10 carbons, and in the alkyl, arbitrary —CH₂— may bereplaced by —O—, —S—, —CO— or —SiH₂—, and arbitrary —(CH₂)₂— may bereplaced by —CH═CH— or —C≡C—; A¹, A², A³ and A⁴ are independently1,4-cyclohexylene, 1,4-phenylene in which one or more of hydrogen isreplaced by halogen, cyclohexene-1,4-diyl, cyclohexene-3,6-diyl,decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,6-diyl ornaphthalene-2,6-diyl, and in the rings, one of —CH₂— may be replaced by—O—, —S—, —CO—, or —SiH₂—, and arbitrary —(CH₂)₂— may be replaced by—CH═CH—, and in the rings, arbitrary hydrogen may be replaced byhalogen, —CF₃, —CHF₂, —CH₂F, —OCF₃, —OCHF₂ or —OCH₂F; and Z¹, Z², Z³ andZ⁴ are independently a single bond or alkylene having 1 to 4 carbons,and in the alkylene, arbitrary —CH₂— may be replaced by —O—, —S— or—SiH₂—, and arbitrary —(CH₂)₂— may be replaced by —CH═CH— or —C≡C—.

A meaning of a phrase “in alkyl, arbitrary —CH₂— may be replaced by —O—,—S—, —CO— or —SiH₂—, and arbitrary —(CH₂)₂— may be replaced by —CH═CH—or —C≡C—” is shown in one example. Specific examples of groups in whicharbitrary —CH₂— in C₄H₉— is replaced by —O— or arbitrary —(CH₂)₂— inC₄H₉ is replaced by —CH═CH— include C₃H₇O—, CH₃—O—(CH₂)₂—, CH₃—O—CH₂—O—,H₂C═CH—(CH₂)₂—, CH₃—CH═CH—CH₂— and CH₂═CH—CH₂—O—. Thus, a term.“arbitrary” means “at least one selected without distinction.” Inconsideration of stability of the compound, CH₃—O—CH₂—O— in which oxygenand oxygen are not adjacent is preferred to CH₃—O—O—CH₂— in which oxygenand oxygen are adjacent.

Preferred R¹ or R² is chlorine, fluorine, alkyl, alkenyl, alkoxy,alkoxyalkyl, alkenyloxy, polyfluoroalkyl, polyfluoroalkoxy andpolyfluoroalkenyl each having 2 to 10 carbons. In the groups, anon-branched chain group is preferred to a branched group. Even if R¹and R² are a branched group, when R¹ and R² are optically active, suchR¹ and R² are preferred. Further preferred R¹ or R² is alkyl, alkenyl,alkoxy, alkoxyalkyl or alkenyloxy each having 2 to 10 carbons. Mostpreferred R¹ and R² are alkyl, alkoxy or alkenyl each having 2 to 10carbons.

A preferred configuration of —CH═CH— in alkenyl depends on a position ofa double bond. A trans configuration is preferred in alkenyl such as1-propenyl, 1-butenyl, 1-pentenyl, 1-hexenyl, 3-pentenyl and 3-hexenyl.A cis configuration is preferred in alkenyl such as 2-butenyl,2-pentenyl and 2-hexenyl.

Specific examples of R¹ or R² include methyl, ethyl, propyl, butyl,pentyl, hexyl, heptyl, octyl, methoxy, ethoxy, propoxy, butoxy,pentyloxy, hexyloxy, heptyloxy, methoxymethyl, methoxyethyl,methoxypropyl, ethoxymethyl, ethoxyethyl, ethoxypropyl, propoxymethyl,butoxymethyl, pentoxymethyl, vinyl, 1-propenyl, 2-propenyl, 1-butenyl,2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl,2-propenyloxy, 2-butenyloxy, 2-pentenyloxy, —CH₂F, —CHF₂, —CF₃,—(CH₂)₂F, —CF₂CH₂F, —CF₂CHF₂, —CH₂CF₃, —CF₂CF₃, —(CH₂)₃F, —(CF₂)₂CF₃,—CF₂CHFCF₃, —CHFCF₂CF₃, —OCF₃, —OCHF₂, —OCH₂F, —OCF₂CF₃, —OCF₂CHF₂,—OCF₂CH₂F, —OCF₂CF₂CF₃, —OCF₂CHFCF₃, —OCHFCF₂CF₃, —CH═CHF, —CH═CF₂,—CF═CHF, —CH═CHCH₂F, —CH═CHCF₃ and —(CH₂)₂CH═CF₂—.

Further preferred R⁴ or R² include fluorine, ethyl, propyl, butyl,pentyl, hexyl, heptyl, octyl, methoxy, ethoxy, propoxy, butoxy,pentyloxy, hexyloxy, heptyloxy, methoxymethyl, methoxyethyl,methoxypropyl, ethoxymethyl, ethoxyethyl, ethoxypropyl, propoxymethyl,butoxymethyl, pentoxymethyl, vinyl, 1-propenyl, 2-propenyl, 1-butenyl,2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl,2-propenyloxy, 2-butenyloxy and 2-pentenyloxy. Most preferred R¹ or R²include ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, methoxy,ethoxy, propoxy, butoxy, pentyloxy, hexyloxy, heptyloxy, vinyl,1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl,2-pentenyl, 3-pentenyl and 4-pentenyl.

A¹, A², A³ and A⁴ are independently 1,4-cyclohexylene, 1,4-phenylene,cyclohexene-1,4-diyl, cyclohexene-3,6-diyl,decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,6-diyl ornaphthalene-2,6-diyl, but when sum of m, n, q, and r is 1, in one ormore of 1,4-phenylene, one or more of hydrogen is replaced by halogenwithout fail, and in the rings, one of —CH₂— may be replaced by —O—,—S—, —CO— or —SiH₂—, and arbitrary —(CH₂)₂— may be replaced by —CH═CH—,and in the rings, one of hydrogen may be replaced by halogen, —CF₃,—CHF₂, —CH₂F, —OCF₃, —OCHF₂ or —OCH₂F.

Preferred A¹, A², A³ and A⁴ are 1,4-cyclohexylene, 1,4-phenylene,cyclohexene-1,4-diyl, cyclohexene-3,6-diyl, 2-fluoro-1,4-phenylene,2,3-difluoro-1,4-phenylene, decahydronaphthalene-2,6-diyl,1,2,3,4-tetrahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl. Furtherpreferred A¹, A², A³ and A⁴ are 1,4-cyclohexylene, 1,4-phenylene,cyclohexene-1,4-diyl, cyclohexene-3,6-diyl, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene and 2,3-difluoro-1,4-phenylene. Most preferredA¹, A², A³ or A⁴ is 1,4-cyclohexylene, 1,4-phenylene and2,3-difluoro-1,4-phenylene.

Z¹, Z², Z³ and Z⁴ are independently a single bond or alkylene having 1to 4 carbons, and in the alkylene, arbitrary —CH₂— may be replaced by—O—, —S— or —SiH₂—, and arbitrary —(CH₂)₂— may be replaced by —CH═CH— or—C═C—.

Preferred Z¹, Z², Z³ and Z⁴ are a single bond, —(CH₂)₂—, —CH═CH—,—CH₂O—, —OCH₂—, —(CH₂)₄—, —C≡C—, —CH₂SiH₂—, —SiH₂CH₂—, —O(CH₂)₂O—,—CH═CH—CH₂O— and —OCH₂—CH═CH—. With regard to a configuration of adouble bond as in —CH═CH—, —CH═CH—CH₂O— and —OCH₂—CH═CH—, trans ispreferred to cis.

Further preferred Z¹, Z², Z³ and Z⁴ are a single bond, —(CH₂)₂—,—CH═CH—, —CH₂O—, —OCH₂—, —(CH₂)₄— and —C≡C—. Most preferred Z¹, Z², Z²,Z³ and Z⁴ are a single bond, —(CH₂)₂—, —CH₂O—, —OCH₂— and —CH═CH—.

Item 2. The compound according to item 1, represented by formula (1-1)to formula (1-8):

wherein, in formula (1-1) to formula (1-8), Ra and Rb are independentlyhydrogen, halogen or alkyl having 1 to 10 carbons, and in the alkyl,arbitrary —CH₂— may be replaced by —O—, —S—, —CO— or —SiH₂—, andarbitrary —(CH₂)₂— may be replaced by —CH═CH— or —C≡C—; A¹¹, A²¹, A³²,A⁴¹, A⁴² and A⁴³ are independently 1,4-cyclohexylene,cyclohexenylene-1,4-diyl, 1,4-phenylene, cyclohexene-3,6-diyl,decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,5-diyl ornaphthalene-2,6-diyl, A³¹ is 1,4-cyclohexylene, cyclohexene-1,4-diyl,1,4-phenylene in which one or more of hydrogen is replaced by halogen,cyclohexene-3,6-diyl, decahydronaphthalene-2,6-diyl,1,2,3,4-tetrahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl, and inthe rings, one of —CH₂— may be replaced by —O—, —S—, —CO—, or —SiH₂—,and arbitrary —(CH₂)₂— may be replaced by —CH═CH—, and in the rings, oneof hydrogen may be replaced by halogen, —CF₃, —CHF₂, —CH₂F, —OCHF₂ or—OCH₂F; and Z¹¹, Z²¹, Z³¹, Z³², Z⁴¹, Z⁴² and Z⁴³ are independently asingle bond or alkylene having 1 to 4 carbons, and in the alkylene,arbitrary —CH₂— may be replaced by —O—, —S— or —SiH₂—, and arbitrary(CH₂)₂— may be replaced by —CH═CH— or

Item 3. The compound according to item 2, wherein, in formula (1-1) toformula (1-8) according to item 2, Ra and Rb are independently fluorine,alkyl having 1 to 10 carbons, alkenyl having 2 to 10 carbons, alkoxyhaving 1 to 9 carbons, alkoxyalkyl having 2 to 9 carbons, alkenyloxyhaving 3 to 9 carbons, polyfluoroalkyl having 2 to 10 carbons,polyfluoroalkoxy having 1 to 9 carbons or polyfluoroalkenyl having 2 to10 carbons; A¹¹, A²¹, A³², A⁴¹, A⁴² and A⁴³ are independently1,4-cyclohexylene, 1,4-phenylene, cyclohexene-1,4-diyl,cyclohexene-3,6-diyl, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene,decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,6-diyl ornaphthalene-2,6-diyl, and A³¹ is 1,4-cyclohexylene,cyclohexene-1,4-diyl, cyclohexene-3,6-diyl, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene, decahydronaphthalene-2,6-diyl,1,2,3,4-tetrahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl; and Z¹¹,Z²¹, Z³¹, Z³², Z⁴¹, Z⁴² and Z⁴³ are independently a single bond,—(CH₂)₂—, —CH═CH—, —CH₂O—, —OCH₂—, —(CH₂)₄—, —CH₂SiH₂—, —SiH₂CH₂—,—O(CH₂)₂O—, —CH═CH—CH₂O— or —OCH₂—CH═CH—.

Item 4. The compound according to item 2, wherein, in formula (1-1) toformula (1-5) according to item 2, Ra and Rb are independently fluorine,alkyl having 1 to 8 carbons, alkenyl having 2 to 8 carbons, alkoxyhaving 1 to 7 carbons, alkoxyalkyl having 2 to 7 carbons or alkenyloxyhaving 3 to 7 carbons; A²¹, A³², A⁴¹ and A⁴² are independently1,4-cyclohexylene, 1,4-phenylene, cyclohexene-1,4-diyl,cyclohexene-3,6-diyl, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene,and A³¹ is 1,4-cyclohexylene, cyclohexene-1,4-diyl,cyclohexene-3,6-diyl, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene;and Z²¹, Z³¹, Z³², Z⁴¹ and Z⁴² are independently a single bond,—(CH₂)₂—, —CH═CH—, —CH₂O—, —OCH₂—, —(CH₂)₄— or —C≡C—.

Item 5. The compound according to item 2, wherein, in formula (1-1) toformula (1-3), Ra and Rb are independently alkyl having 1 to 5 carbons,alkenyl having 2 to 5 carbons or alkoxy having 1 to 4 carbons; A²¹, A³¹,A³² and A⁴² are independently 1,4-cyclohexylene; and Z²¹, Z³¹, Z³² andZ⁴² are independently a single bond, —(CH₂)₂— or —CH═CH—.

Item 6. The compound according to item 2, wherein, in formula (1-1) toformula (1-3), A²¹, A³¹, A³² and A⁴² are independently1,4-cyclohexylene, and Z²¹, Z³¹, Z³² and Z⁴² are a single bond.

Item 7. The compound according to item 1, represented by formula (1-1)to formula (1-8):

wherein, in formula (1-1) to formula (1-8), Ra and Rb are independentlyalkyl having 1 to 10 carbons, alkenyl having 2 to 10 carbons, alkoxyhaving 1 to 9 carbons, alkoxyalkyl having 2 to 9 carbons, alkenyloxyhaving 3 to 9 carbons, polyfluoroalkyl having 2 to 10 carbons,polyfluoroalkoxy having 1 to 9 carbons or polyfluoroalkenyl having 2 to10 carbons; A¹¹, A²¹, A³¹, A³², A⁴¹, A⁴² and A⁴³ are independently1,4-cyclohexylene, 1,4-phenylene, cyclohexene-1,4-diyl,cyclohexene-3,6-diyl, tetrahydropyran-2,5-diyl, 1,3-dioxane-2,5-diyl,2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene,2,3-difluoro-1,4-phenylene, 2-(trifluoromethyl)-3-fluoro-1,4-phenylene,2-fluoro-3-(trifluoromethyl)-1,4-phenylene,2-(difluoromethyl)-3-fluoro-1,4-phenylene,2-fluoro-3-(difluoromethyl)-1,4-phenylene,2-trifluoromethyl-1,4-phenylene, 3-trifluoromethyl-1,4-phenylene,2-difluoromethyl-1,4-phenylene, 3-difluoromethyl-1,4-phenylene,decahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl, but at least oneof A¹¹, A²¹, A³¹, A³², A⁴¹, A⁴² and A⁴³ is 2,3-difluoro-1,4-phenylene,2-(trifluoromethyl)-3-fluoro-1,4-phenylene,2-fluoro-3-(trifluoromethyl)-1,4-phenylene,2-(difluoromethyl)-3-fluoro-1,4-phenylene or2-fluoro-3-(difluoromethyl)-1,4-phenylene; and Z¹¹, Z²¹, Z³¹, Z³², Z⁴¹,Z⁴², and Z⁴³ are independently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O—,—OCH₂—, —(CH₂)₄—, —C≡C—, —CH₂SiH₂—, —SiH₂CH₂—, —CH═CH—CH₂O— or—OCH₂—CH═CH—.

Item 8. The compound according to item 7, wherein, in formula (1-1) toformula (1-5), Ra and Rb are independently fluorine, alkyl having 1 to 8carbons, alkenyl having 2 to 8 carbons, alkoxy having 1 to 7 carbons,alkoxyalkyl having 2 to 7 carbons or alkenyloxy having 3 to 7 carbons;A²¹, A³¹, A³², A⁴¹ and A⁴² are independently 1,4-cyclohexylene,1,4-phenylene, cyclohexene-1,4-diyl, tetrahydropyran-2,5-diyl,2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene,2,3-difluoro-1,4-phenylene, 2-(trifluoromethyl)-3-fluoro-1,4-phenylene,2-fluoro-3-(trifluoromethyl)-1,4-phenylene,2-(difluoromethyl)-3-fluoro-1,4-phenylene or2-fluoro-3-(difluoromethyl)-1,4-phenylene, but at least one of A²¹, A³¹,A³², A⁴¹ and A⁴² is 2,3-difluoro-1,4-phenylene,2-(trifluoromethyl)-3-fluoro-1,4-phenylene,2-fluoro-3-(trifluoromethyl)-1,4-phenylene,2-(difluoromethyl)-3-fluoro-1,4-phenylene or2-fluoro-3-(difluoromethyl)-1,4-phenylene; and Z²¹, Z³¹, Z³², Z⁴¹ andZ⁴² are independently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O—, —OCH₂—,—(CH₂)₄— or —C≡C—.

Item 9. The compound according to item 7, wherein, in formula (1-1) toformula (1-5), Ra and Rb are independently alkyl having 1 to 5 carbons,alkenyl having 2 to 5 carbons or alkoxy having 1 to 4 carbons; A²¹, A³¹,A³², A⁴¹ and A⁴² are independently 1,4-cyclohexylene, 1,4-phenylene,2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene or2,3-difluoro-1,4-phenylene, but at least one of A²¹, A³¹, A³², A⁴¹ andA⁴² is 2,3-difluoro-1,4-phenylene; and Z²¹, Z³¹, Z³², Z⁴¹ and Z⁴² areindependently a single bond, —(CH₂)₂—, —CH₂O—, —OCH₂— or —CH═CH—.

Item 10. The compound according to item 7, wherein, in formula (1-1) toformula (1-3), A²¹, A³¹, A³² and A⁴² are independently1,4-cyclohexylene, 1,4-phenylene or 2,3-difluoro-1,4-phenylene, but atleast one of A²¹, A³¹, A³² and A⁴² is 2,3-difluoro-1,4-phenylene, andZ²¹, Z³¹, Z³² and Z⁴² are a single bond, —CH₂O— or —OCH₂—.

Item 11. The compound according to item 2, represented by any one offormula (1-1-1) to formula (1-1-2), formula (1-2-1) to formula (1-2-4),formula (1-3-1) to formula (1-3-3), formula (1-4-1) to formula (1-4-6)and formula (1-5-1) to formula (1-5-7):

wherein, in formula (1-1-1), formula (1-2-1) to formula (1-2-4), formula(1-3-1) to formula (1-3-3), formula (1-4-1) to formula (1-4-6) andformula (1-5-1) to formula (1-5-7), Ra and Rb are independently alkylhaving 2 to 10 carbons, alkoxy having 1 to 9 carbons or alkenyl having 2to 10 carbons; Z²¹, Z³¹, Z³², Z⁴¹ and Z⁴² are independently a singlebond, —(CH₂)₂—, —CH═CH—, —CH₂O—, —OCH₂—, —CF₂O— or —OCF₂—; X¹² to X¹⁴,X²² to X²⁴, X³² to X³⁴ and X⁴² to X⁴⁴ are independently fluorine orhydrogen; in formula (1-1-2), R³ and R⁴ are independently alkyl having 1to 10 carbons, alkenyl having 2 to 10 carbons, alkoxy having 1 to 9carbons, alkoxyalkyl having 2 to 9 carbons or alkenyloxy having 2 to 9carbons; X¹⁰, X²⁰, X³⁰ and X⁴⁰ are independently hydrogen or fluorine,and at least one of X¹⁰, X²⁰, X³⁰ and X⁴⁰ is fluorine; and Z³¹ is asingle bond, —(CH₂)₂—, —CH═CH—, —CH₂O—, —OCH₂—, —CF₂O—Or —OCF₂—.

Item 12. The compound according to item 2, represented by any one offormulas (1-1-1), (1-2-1) and (1-3-1):

wherein, in formulas (1-1-1), (1-2-1) and (1-3-1), Ra and Rb areindependently alkyl having 1 to 8 carbons, alkoxy having 1 to 7 carbonsor alkenyl having 2 to 8 carbons; and Z²¹, Z³¹, Z³² and Z⁴¹ areindependently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—.

Item 13. The compound according to item 12, wherein, in formulas(1-1-1), (1-2-1) and (1-3-1), Ra and Rb are alkyl having 1 to 5 carbonsor alkenyl having 2 to 5 carbons; and Z²¹, Z³², Z³² and Z⁴¹ areindependently a single bond or —CH═CH—.

Item 14. The compound according to item 12, wherein, in formulas(1-1-1), (1-2-1) and (1-3-1), one of Ra and Rb is alkenyl having 2 to 5carbons; and Z²¹, Z³¹, Z³² and Z⁴² are independently a single bond or—CH═CH—.

Item 15. The compound according to item 12, wherein, in formulas(1-1-1), (1-2-1) and (1-3-1), Ra and Rb are alkenyl having 2 to 5carbons, and Z²¹, Z³¹, Z³² and Z⁴¹ are independently a single bond or—CH═CH—.

Item 16. The compound according to item 7, represented by any one offormula (1-1-2), formula (1-2-2) to formula (1-2-4), formula (1-3-2),formula (1-3-3), formula (1-4-2) to formula (1-4-6) and formula (1-5-2)to formula (1-5-7):

wherein, in formula (1-1-2), formula (1-2-2) to formula (1-2-4), formula(1-3-2) to formula (1-3-3), formula (1-4-2) to formula (1-4-6) andformula (1-5-2) to formula (1-5-7), Ra and Rb are independently alkylhaving 2 to 10 carbons, alkoxy having 1 to 9 carbons or alkenyl having 2to 10 carbons; X¹⁰, X²⁰, X¹², X²², X¹³, X²³, X¹⁴ and X²⁴ areindependently fluorine or hydrogen, but both in at least one set of X¹⁰and X²⁰, X¹² and X²², X¹³ and X²³, and X¹⁴ and X²⁴ are fluorine; Z²¹,Z³¹, Z³², Z⁴¹ and Z⁴² are independently a single bond, —(CH₂)₂—,—CH═CH—, —CH₂O— or —OCH₂—.

Item 17. The compound according to item 7, represented by any one offormulas (1-1-2), (1-2-2) to (1-2-4), and (1-3-3):

wherein, in formulas (1-1-2), (1-2-2) to (1-2-4), and (1-3-3), Ra and Rbare independently alkyl having 1 to 8 carbons, alkoxy having 1 to 7carbons or alkenyl having 2 to 8 carbons; X¹⁰, X²⁰, X¹², X²², X¹³, X²³,X¹⁴ and X²⁴ are independently fluorine or hydrogen, but both in at leastone set of X¹⁰ and X²⁰, X¹² and X²², X¹³ and X²³, and X¹⁴ and X²⁴ arefluorine; Z²¹, Z³¹, Z³² and Z⁴¹ are independently a single bond,—(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—.

Item 18. The compound according to item 17, wherein, in formulas(1-1-2), (1-2-3) and (1-2-4), Ra and Rb are alkyl having 1 to 5 carbons,alkoxy having 1 to 5 carbons or alkenyl having 2 to 5 carbons; X¹⁰, X²⁰,X¹⁴ and X²⁴ are fluorine, X¹³ and X²³ are independently fluorine orhydrogen; and Z²¹, Z³¹, Z³² and Z⁴¹ are independently a single bond,—CH═CH—, —CH₂O— or —OCH₂—.

Item 19. The compound according to item 17, wherein, in formulas(1-1-2), (1-2-3) and (1-2-4), Ra and Rb are alkyl having 1 to 5 carbons,alkoxy having 1 to 5 carbons or alkenyl having 2 to 5 carbons; X¹⁰, X²⁰,X¹⁴ and X²⁴ are fluorine, and X¹³ and X²³ are independently fluorine orhydrogen; and Z²¹, Z³¹, Z³² and Z⁴² are independently a single bond,—CH₂O— or —OCH₂—.

Item 20. The compound according to item 17, wherein, in formulas(1-1-2), (1-2-3) and (1-2-4), Ra and Rb are alkyl having 1 to 5 carbons,alkoxy having 1 to 5 carbons or alkenyl having 2 to 5 carbons; X¹⁰, X²⁰,X¹⁴ and X²⁴ are fluorine, and X¹³ and X²³ are hydrogen; and Z²¹, Z³¹,Z³² and Z⁴¹ are independently a single bond or —CH₂O—.

Item 21. A liquid crystal composition containing at least one compoundaccording to any one of items 1 to 20.

Item 22. The liquid crystal composition according to item 21, furthercontaining at least one compound selected from the group of compoundsrepresented by formulas (2), (3) and (4):

wherein, in formulas (2) to (4), R⁹ is independently alkyl having 1 to10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and thealkenyl, arbitrary hydrogen may be replaced by fluorine and arbitrary—CH₂— may be replaced by —O—;

X² is fluorine, chlorine, —OCF₃, —OCHF₂, —CF₃, —CHF₂, —CH₂F, —OCF₂CHF₂or —OCF₂CHFCF₃;

ring B¹, ring B² and ring B³ are independently 1,4-cyclohexylene,1,3-dioxane-2,5-diyl, pyrimidine-2,5-diyl, tetrahydropyran-2,5-diyl,1,4-phenylene, 2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene or3,5-difluoro-1,4-phenylene;

Z⁷ and Z⁸ are independently —(CH₂)₂—, —(CH₂)₄—, —COO—, —CF₂O—, —OCF₂—,—CH═CH—, —C≡C—, —CH₂O— or a single bond; and

L⁹ and L¹⁰ are independently hydrogen or fluorine.

Item 23. The liquid crystal composition according to item 21, furthercontaining at least one compound selected from the group of compoundsrepresented by formula (5):

wherein, in formula (5), R¹⁰ is alkyl having 1 to 10 carbons or alkenylhaving 2 to 10 carbons, and in the alkyl and the alkenyl, arbitraryhydrogen may be replaced by fluorine and arbitrary —CH₂— may be replacedby —O—;

X² is —C≡N or —C≡C—C≡N;

ring C¹, ring C² and ring C³ are independently 1,4-cyclohexylene,1,4-phenylene in which arbitrary hydrogen may be replaced by fluorine,1,3-dioxane-2,5-diyl, tetrahydropyran-2,5-diyl or pyrimidine-2,5-diyl;

Z⁹ is —(CH₂)₂—, —COO—, —CF₂O—, —OCF₂—, —C≡C—, —CH₂O— or a single bond;

L¹¹ and L¹² are independently hydrogen or fluorine; and

o is 0, 1 or 2, p is 0 or 1, and a sum of o and p is 0, 1, 2 or 3.

Item 24. The liquid crystal composition according to item 21, furthercontaining at least one compound selected from the group of compoundsrepresented by formulas (6), (7), (8), (9), (10) and (11):

wherein, in formulas (6) to (11), R¹¹ and R¹² are independently alkylhaving 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in thealkyl and the alkenyl, arbitrary hydrogen may be replaced by fluorineand arbitrary —CH₂— may be replaced by —O—;

ring D¹, ring D², ring D³ and ring D⁴ are independently1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene in which arbitraryhydrogen may be replaced by fluorine, 6-tetrahydropyran-2,5-diyl ordecahydro-2,6-naphthalene;

Z¹⁰, Z¹¹, Z¹² and Z¹³ are independently —(CH₂)₂—, —COO—, —CH₂O—, —OCF₂—,—OCF₂(CH₂)₂— or a single bond;

L¹³ and L¹⁴ are independently fluorine or chlorine; and

q, r, s, t, u and v are independently 0 or 1, and a sum of r, s, t and uis 1 or 2.

Item 25. The liquid crystal composition according to item 21, furthercontaining at least one compound selected from the group of compoundsrepresented by formulas (12), (13) and (14):

wherein, in formulas (12) to (14), R¹³ and R¹⁴ are independently alkylhaving 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in thealkyl and the alkenyl, arbitrary —CH₂— may be replaced by —O—;

ring E¹, ring E² and ring E³ are independently 1,4-cyclohexylene,pyrimidine-2,5-diyl, 1,4-phenylene, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; and

Z¹⁴ and Z¹⁵ are independently —C≡C—, —COO—, —(CH₂)₂—, —CH═CH— or asingle bond.

Item 26. The liquid crystal composition according to item 22, furthercontaining at least one compound selected from the group of compoundsrepresented by formula (5) according to item 23.

Item 27. The liquid crystal composition according to item 22, furthercontaining at least one compound selected from the group of compoundsrepresented by formulas (12), (13) and (14) according to item 25.

Item 28. The liquid crystal composition according to item 23, furthercontaining at least one compound selected from the group of compoundsrepresented by formulas (12), (13) and (14) according to item 25.

Item 29. The liquid crystal composition according to item 24, furthercontaining at least one compound selected from the group of compoundsrepresented by formulas (12), (13) and (14) according to item 25.

Item 30. The liquid crystal composition according to any one of items 21to 29, further containing at least one optically active compound and/orat least one polymerizable compound.

Item 31. The liquid crystal composition according to any one of items 21to 30, further containing at least one antioxidant and/or at least oneultraviolet light absorber.

Item 32. A liquid crystal display device including the liquid crystalcomposition according to any one of items 21 to 31.

Advantageous Effects of Invention

A compound of the invention has both a high clearing point and a lowcrystallization temperature, and thus has a wide temperature range of aliquid crystal phase, and an excellent solubility in other liquidcrystal compounds. The compound of the invention has general physicalproperties necessary for the compound, namely, stability to heat, lightand so forth, a suitable optical anisotropy and a suitable dielectricanisotropy. A liquid crystal composition of the invention contains atleast one of the compounds, and has a high maximum temperature of anematic phase, a low minimum temperature of the nematic phase, a smallviscosity, a suitable optical anisotropy and a low threshold voltage. Aliquid crystal display device of the invention includes the composition,and has a wide temperature range in which the device can be used, ashort response time, a large contrast ratio and a low driving voltage.

DESCRIPTION OF EMBODIMENTS

Usage of terms herein is as described below. A liquid crystal compoundis a generic term for a compound having a liquid crystal phase such as anematic phase and a smectic phase and a compound having no liquidcrystal phase but being useful as a component of the liquid crystalcomposition. “Liquid crystal compound,” “liquid crystal composition” and“liquid crystal display device” may be occasionally abbreviated as“compound,” “composition,” and “device,” respectively. The liquidcrystal display device is a generic term for a liquid crystal displaypanel and a liquid crystal display module. A maximum temperature of thenematic phase is a phase transition temperature between the nematicphase and an isotropic phase, and may be occasionally abbreviated simplyas “maximum temperature.” A minimum temperature of the nematic phase maybe occasionally abbreviated simply as “minimum temperature.” A compoundrepresented by formula (1) may be occasionally abbreviated as compound(1). The abbreviation may be occasionally applied to a compoundrepresented by formula (2), or the like. In formulas (1) to (14), asymbol such as A¹ and A² corresponds to each of ring A¹, ring B¹, ringE, ring M, or the like. A ratio (percentage) of components or liquidcrystal compounds is expressed in terms of weight percent (% by weight)based on the total weight of liquid crystal compound. Hereinafter, theinvention will be further explained.

First, compound (1) of the invention will be further explained. A fusedring such as a naphthalene ring is counted to be a monocycle. Compound(1) includes a bicyclic compound, a tricyclic compound, a tetracycliccompound and a pentacyclic compound each having a cyclohexene-3,6-diylring. The compound is physically and chemically stable under conditionsin which the device is ordinarily used, and has a good solubility inother liquid crystal compounds. A composition containing the compound isstable under conditions in which the device is ordinarily used. Even ifthe composition is stored at a low temperature, the compound does notprecipitate as crystals (or smectic phase). The compound has generalphysical properties necessary for the compound, namely, a suitableoptical anisotropy and a suitable dielectric anisotropy.

Physical properties of compound (1), such as optical anisotropy, can bearbitrarily adjusted by suitably selecting a terminal group, a ring anda bonding group of compound (1). An effect of types of terminal groupsR² and R², rings A¹, A², A³ and A⁴, bonding groups Z¹, Z², Z³ and Z⁴ onphysical properties of compound (1) will be explained below.

When Ra or Rb is a non-branched chain, a temperature range of the liquidcrystal phase is wide, and viscosity is small. When Ra or Rb is abranched chain, solubility in other liquid crystal compounds issatisfactory. A compound in which Ra or Rb is an optically active groupis useful as a chiral dopant. A reverse twisted domain generated in thedevice can be prevented by adding the compound to the composition. Acompound in which Ra or Rb is not the optically active group is usefulas a component of the composition. When Ra or Rb is alkenyl, a preferredconfiguration depends on a position of a double bond. An alkenylcompound having a preferred configuration has a high maximum temperatureor a wide temperature range of the liquid crystal phase. A detaileddescription is found in Mol. Cryst. Liq. Cryst., 1985, 131, 109 and Mol.Cryst. Liq. Cryst., 1985, 131, 327.

When rings A¹ to A⁴ are 1,4-phenylene, 2-fluoro-1,4-phenylene or3-fluoro-1,4-phenylene, the optical anisotropy is large. When rings A¹to A⁴ are 1,4-cyclohexylene, the optical anisotropy small.

When at least two rings are 1,4-cyclohexylene, the maximum temperatureis high, the optical anisotropy is small and the viscosity is small.When at least one ring is 1,4-phenylene, the optical anisotropy isrelatively large and an orientational order parameter is large.

When rings A¹ to A⁴ are 1,4-phenylene in which arbitrary hydrogen isreplaced by halogen, pyridine-2,5-diyl or 1,3-dioxane-2,5-diyl,dielectric anisotropy is positively large. When rings A¹ to A⁴ are2,3-difluoro-1,4-phenylene, the dielectric anisotropy is negativelylarge. When rings A¹ to A⁴ are2-(trifluoromethyl)-3-fluoro-1,4-phenylene,2-fluoro-3-(trifluoromethyl)-1,4-phenylene,2-(difluoromethyl)-3-fluoro-1,4-phenylene or2-fluoro-3-(difluoromethyl)-1,4-phenylene, the dielectric anisotropy isfurther negatively large. When rings A¹ to A⁴ are 1,4-phenylene in whicharbitrary hydrogen may be replaced by halogen, pyridine-2,5-diyl,pyrimidine-2,5-diyl or pyridazine-3,6-diyl, the optical anisotropy islarge. When ring A¹ or A² is 1,4-cyclohexylene, 1,4-cyclohexenylene or1,3-dioxane-2,5-diyl, the optical anisotropy is small.

When rings A¹ to A⁴ are cyclohexene-1,4-diyl or cyclohexene-3,6-diyl, amelting point is low. In particular, in a case of cyclohexene-3,6-diyl,the temperature range of the liquid crystal phase is wide, and acrystallization temperature is low. When a compound simultaneously hascyclohexene-1,4-diyl and 1,4-phenylene, the optical anisotropy is large.

When bonding group Z¹, Z², Z³ or Z⁴ is a single bond, —(CH₂)₂—, —CH₂O—,—CH═CH— or —(CH₂)₄—, the viscosity is small. When the bonding group is asingle bond, —(CH₂)₂— or —CH═CH—, the viscosity is further smaller. Whenthe bonding group is —CH═CH—, the temperature range of the liquidcrystal phase is wide, and an elastic constant ratio K₃₃/K₁₁ (K₃₃: bendelastic constant, K₁₁: spray elastic constant) is large. When thebonding group is —C≡C—, the optical anisotropy is large.

When compound (1) has abicyclic or tricyclic structure, the viscosity issmall. When compound (1) has a tricyclic or tetracyclic structure, themaximum temperature is high. As described above, a compound havingobjective physical properties can be obtained by suitably selecting thetypes of terminal groups, rings and bonding groups, and the number ofrings. Accordingly, compound (1) is useful as a component of thecomposition used for a device according to PC, TN, STN, ECB, OCB, IPS,VA or the like.

Preferred examples of compound (1) include compounds represented byformulas (1-1) to (1-8) according to item 2 of the invention. SymbolsRa, Rb, A¹¹, A²¹, A³¹ to A³² and A⁴¹ to A⁴³, Z¹¹, Z²¹, Z³¹ to Z³², andZ⁴¹ to Z⁴³ in the compounds are defined in a manner identical with thedefinitions of symbols as described in item 2.

Compound (1) is synthesized by suitably combining techniques insynthetic organic chemistry. Methods for introducing an objectiveterminal group, ring, and bonding group into a starting material aredescribed in books such as Organic Syntheses (John Wiley & Sons, Inc.),Organic Reactions (John Wiley & Sons, Inc), Comprehensive OrganicSynthesis (Pergamon Press) and New Experimental Chemistry Course (ShinJikken Kagaku Koza in Japanese) (Maruzen Co., Ltd.).

With regard to one example of a method for forming bonding groups Z¹, Z²or Z⁴, a scheme is first shown, and next each scheme will be explainedin sections (I) to (XI). In the scheme, MSG¹ or MSG² is a monovalentorganic group having at least one ring. A plurality of organic groupsrepresented by MSG¹ (or MSG²) may be identical or different. Compounds(1A) to (1K) correspond to compound (1).

(I) Formation of a Single Bond

Compound (1A) is prepared by allowing arylboronic acid (21) to react, inthe presence of an aqueous solution of carbonate and a catalyst such astetrakis(triphenylphosphine)palladium, with compound (22) to be preparedaccording to a publicly known method. Compound (1A) is also prepared byallowing compound (23) prepared according to a publicly known method toreact with n-butyllithium and subsequently with zinc chloride, andfurther with compound (22) in the presence of a catalyst such asdichlorobis(triphenylphosphine)palladium.

(II) Formation of —COO— and —OCO—

Carboxylic acid (24) is obtained by allowing compound (23) to react withn-butyllithium, and subsequently with carbon dioxide. Compound (1B)having —COO— is prepared by dehydrating, in the presence of1,3-dicyclohexylcarbodiimide (DDC) and 4-dimethylaminopyridine (DMAP),compound (24) and phenol (25) prepared according to a publicly knownmethod. A compound having —OCO— is also prepared according to themethod.

(III) Formation of —CF₂O— and —OCF₂—

Compound (26) is obtained by treating compound (1B) with a thiationreagent such as Lawesson's reagent. Compound (1C) having —CF₂O— isprepared by fluorinating compound (26) with a hydrogen fluoride pyridinecomplex and N-bromosuccinimide (NBS). See M. Kuroboshi et al., Chem.Lett., 1992, 827. Compound (1C) is also prepared by fluorinatingcompound (26) with (diethylamino)sulfur trifluoride (DAST). See W. H.Bunnelle et al., J. Org. Chem. 1990, 55, 768. A compound having —OCF₂—is also prepared according to the method. The bonding groups can also beformed according to the method described in Peer. Kirsch et al., Angew.Chem. Int. Ed. 2001, 40, 1480.

(IV) Formation of —CH═CH—

Aldehyde (28) is obtained by treating compound (23) with n-butyllithiumand then allowing a treated compound to react with formamide such asN,N-dimethylformamide (DMF). Compound (1D) is prepared by allowingphosphorus ylide generated by treating phosphonium salt (27) preparedaccording to a known method with a base such as potassium tert-butoxideto react with aldehyde (28). Because a cis isomer is formed depending onreaction conditions, the cis isomer is isomerized into a trans isomeraccording to a known method, when necessary.

(V) Formation of —(CH₂)₂—

Compound (1E) is prepared by hydrogenating compound (1D) in the presenceof a catalyst such as palladium on carbon.

(VI) Formation of —(CH₂)₄—

A compound having —(CH₂)₂—CH═CH— is obtained by using phosphonium salt(29) in place of phosphonium salt (27) according to the method insection (IV). Compound (1F) is prepared by performing catalytichydrogenation of the compound obtained.

(VII) Formation of —C≡C—

Compound (30) is obtained by allowing compound (23) to react with2-methyl-3-butyn-2-ol in the presence of a catalyst includingdichloropalladium and copper halide, and then performing deprotectionunder basic conditions. Compound (1G) is prepared by allowing compound(30) to react with compound (22) in the presence of a catalyst includingdichloropalladium and copper halide.

(VIII) Formation of —CF═CF—Compound (31) is obtained by treatingcompound (23) with n-butyllithium and then allowing a treated compoundto react with tetrafluoroethylene. Compound (1H) is prepared by treatingcompound (22) with n-butyllithium and then allowing a treated compoundto react with compound (31).

(IX) Formation of —CH₂O— or —OCH₂—

Compound (32) is obtained by reducing compound (28) with a reducingagent such as sodium borohydride. Compound (33) is obtained byhalogenating compound (32) with hydrobromic acid or the like. Compound(1J) is prepared by allowing compound (33) to react with compound (25)in the presence of potassium carbonate or the like.

(X) Formation of —(CH₂)₃O— or —O(CH₂)₃—

Compound (1K) is prepared by using compound (29) in place of compound(32) in a manner similar to section (IX).

(X¹) Formation of —(CF₂)₂—

A compound having —(CF₂)₂— is obtained by fluorinating, in the presenceof a hydrogen fluoride catalyst, diketone (—COCO—) with sulfurtetrafluoride according to the method described in J. Am. Chem. Soc.,2001, 123, 5414.

One example of a method for synthesizing compound (1) is shown in ascheme as described below. A scheme for synthesizing syntheticintermediate (38) having cyclohexene-3,6-diyl will be first explained,and one example of a method for synthesizing cyclohexene-3,6-diylcompound (41) in which (38) is used as a starting material will then bedescribed.

In compounds (36) to (38), Q¹ is a structural unit in formula (1). Thestructural unit is shown in the scheme. Symbols Ra, A¹, A², m, n, Z¹ andZ² in the compounds are defined in a manner identical with thedefinitions of symbols as described in item 1.

Compound (37) is prepared by allowing LDA to act on compound (36) toform an enolate, and then allowing trimethylsilyl chloride to actthereon. The reactions are preferably performed in a solvent such asTHF, in the presence of a bulky strong base such as LDA that selectivelyperforms deprotonation, and at a low temperature, namely, at roomtemperature or lower. Compound (38) is prepared by allowing palladiumacetate and 1,4-benzoquinone to act on compound (37). As an alternativemethod, compound (38) can also be prepared by an oxidization reactionusing OXONE (registered tradename) and using a 2-iodosulfonic acidderivative such as sodium 2-iodosulfonate as a catalyst. In addition,compound (36) being a starting material can be easily prepared accordingto a method of synthetic organic chemistry.

Next, one example of a synthetic process of compound (41) is shown.

In compounds (38) to (41), Q¹ or Q² is a structural unit in formula (1).The structural unit is shown in the scheme. Symbols Ra, Rb, A¹ to A⁴, Z²to Z⁴, m, n, q and r in the compounds are defined in a manner identicalwith the definitions of symbols as described in item 1.

Compound (40) is prepared by a reaction between compound (38) andcompound (39). The reaction is preferably performed in an ether solventsuch as tetrahydrofuran at a temperature in the range of 50° C. to 30°C. Compound (41) is prepared by allowing compound (40) to react in asolvent such as dichloromethane in the presence of triethylsilane and aboron trifluoride-diethyl ether complex at a temperature of −50° C. orlower. In addition, compound (39) can be easily prepared according to amethod of synthetic organic chemistry.

Next, one example of a method for synthesizing cyclohexene-3,6-diylcompound (44) will be described.

In compounds (38), and (42) to (44), Q¹ or Q² is a structural unit informula (1). The structural unit is shown in the scheme. Symbols Ra, Rb,A¹ to A⁴, Z² to Z⁴, m, n, q and r are defined in a manner identical withthe definitions of symbols as described in item 1.

Compound (42) is obtained by reducing compound (38) with DIBAL-H or thelike. The reaction is preferably performed in a solvent such as tolueneat a temperature of −60° C. or lower. Compound (44) is prepared byallowing compound (42) to react with compound (43) in the presence ofpotassium carbonate or the like. In addition, compound (43) can beeasily prepared according to a method of synthetic organic chemistry.

Liquid Crystal Composition

Hereinafter, the liquid crystal composition of the invention will beexplained. The component of the liquid crystal composition ischaracterized by containing at least one compound (1). The compositionmay contain two or more compounds (1), and may be constituted of onlycompound (1). Moreover, when preparing the liquid crystal composition ofthe invention, a component can also be selected, for example, inconsideration of the dielectric anisotropy of compound (1). Thecomposition prepared by selecting the component has a low viscosity, asuitable dielectric anisotropy and a low threshold voltage, and also ahigh maximum temperature of the nematic phase, and a low minimumtemperature of the nematic phase.

Liquid Crystal Composition (1)

The liquid crystal composition of the invention needs to containcompound (1) as component A. The liquid crystal composition of theinvention may include a composition of only component A or a compositionof component A with any other component whose component name is notparticularly shown herein, but a liquid crystal composition havingvarious characteristics can be provided by adding to component A acomponent selected from components B, C, D and E shown below.

As the component to be added to component A, the liquid crystalcomposition of the invention preferably contains a mixture containingcomponent B including at least one compound selected from the group ofcompounds represented by formulas (2), (3) and (4), and/or component Cincluding at least one compound selected from the group of compoundsrepresented by formula (5), and/or component D including at least onecompound selected from the group of compounds represented by formulas(6), (7), (8), (9), (10) and (11). Furthermore, when component Eincluding at least one compound selected from the group of compoundsrepresented by formulas (12), (13) and (14) is mixed, a thresholdvoltage, the temperature range of the liquid crystal phase, refractiveindex anisotropy, the dielectric anisotropy, the viscosity or the likecan be adjusted.

Moreover, the liquid crystal composition of the invention does not havea large difference in physical properties even when each component ofthe liquid crystal composition used in the invention is constituted ofan analog including an isotopic element of each element.

Among types of component B, suitable examples of compounds representedby formula (2) include compounds (2-1) to (2-16), suitable examples ofcompounds represented by formula (3) include compounds (3-1) to (3-112),and suitable examples of compounds represented by formula (4) includecompounds (4-1) to (4-54).

In the formulas, R⁹ and X¹ are defined in a manner identical with thedefinitions as described above.

Components represented by formulas (2) to (4), namely, component B, havea positive dielectric anisotropy, and a superb thermal and chemicalstability, and therefore are used when preparing a liquid crystalcomposition for TFT and PSA. Content of component B in the liquidcrystal composition of the invention is suitably in the range of 1 to99% by weight, preferably, in the range of 10 to 97% by weight, furtherpreferably, 40 to 95% by weight, based on the total weight of liquidcrystal composition. Moreover, when compounds represented by formulas(12) to (14) (component E) are further introduced into the composition,the viscosity can be controlled.

Suitable examples of compounds represented by formula (5), namely,component C, include compounds represented by formulas (5-1) to (5-64).

In the formulas, R¹⁰ and X² are defined in a manner identical with thedefinitions as described above.

In formula (5), two of ring C² when o is 2 may be identical ordifferent.

Components represented by formula (5), namely, component C, have apositive dielectric anisotropy and a very large value, and therefore aremainly used when preparing a liquid crystal composition for STN, TN orPSA. When the component C is introduced into the composition, thethreshold voltage of the composition can be decreased. Moreover, theviscosity and the refractive index anisotropy can be adjusted, and thetemperature range of the liquid crystal phase can be extended. Moreover,the composition can be also used for improvement in steepness.

When preparing a liquid crystal composition for STN or TN, content ofcomponent C is suitably in the range of 0.1 to 99.9% by weight,preferably, in the range of 10 to 97% by weight, further preferably, 40to 95% by weight, based on the total weight of liquid crystalcomposition. Moreover, when a component as described layer is mixed, thethreshold voltage, the temperature range of the liquid crystal phase,the refractive index anisotropy, the dielectric anisotropy, theviscosity or the like can be adjusted.

Component D including at least one kind compound selected from the groupof compounds represented by formulas (6) to (11) is preferred whenpreparing a liquid crystal composition having a negative dielectricanisotropy used for a vertical alignment mode (VA mode) and a polymersustained alignment mode (PSA mode) and so forth.

Suitable examples of compounds represented by formulas (6) to (11)(component D) include compounds represented by formulas (6-1) to (6-6),(7-1) to (7-15), (8-1), (9-1) to (9-3), (10-1) to (10-11), and (11-1) to(11-10), respectively.

In the formulas, R¹¹ and R¹² are defined in a manner identical with thedefinitions as described above.

The compounds of component D are used mainly for a liquid crystalcomposition having a negative dielectric anisotropy for the VA mode orthe PSA mode. If the content thereof is increased, the threshold voltageof the composition decreases, but the viscosity increases, and thereforethe content is preferably as small as possible, as long as a requirementfor the threshold voltage is met. However, an absolute value ofdielectric anisotropy is about 5, and therefore the content ispreferably 40% by weight or more in order to perform sufficient voltagedriving.

Among types of component D, the compound represented by formula (6) is abicyclic compound, and therefore effective mainly in adjusting thethreshold voltage, the viscosity or the refractive index anisotropy.Moreover, the compounds represented by formula (7) and formula (8) eachare a tricyclic compound, and therefore effective in increasing theclearing point, extending the temperature range of the nematic phase,decreasing the threshold voltage, increasing the refractive indexanisotropy, or the like. Moreover, the compounds represented by formulas(9), (10) and (11) are effective in decreasing the threshold voltage.

When preparing a liquid crystal composition for the VA mode or the PSAmode, content of component D is preferably 40% by weight or more,further preferably, in the range of 50 to 95% by weight, based on thetotal weight of liquid crystal composition. Moreover, when component Dis mixed, the elastic constant can be controlled, and avoltage-transmittance curve of the composition. When component D ismixed with a composition having a positive dielectric anisotropy, thecontent thereof is preferably 30% by weight or less based on the totalamount of the composition.

Suitable examples of compounds represented by formulas (12), (13) and(14) (component E) include compounds represented by formulas (12-1) to(12-11), (13-1) to (13-19), and (14-1) to (14-6), respectively.

In the formulas, R¹³ and R¹⁴ are defined in a manner identical with thedefinitions as described above.

The compounds represented by formulas (12) to (14) (component E) eachhave a small absolute value of dielectric anisotropy, and close toneutrality. The compound represented by formula (12) is effective mainlyin adjusting the viscosity and the refractive index anisotropy, and thecompounds represented by formulas (13) and (14) are effective inextending the temperature range of the nematic phase, such as increasingthe clearing point, or adjusting the refractive index anisotropy.

If content of the compound represented by component E is increased, thethreshold voltage of the liquid crystal composition increases, and theviscosity decreases, and therefore content thereof is desirably as highas possible, as long as a required value of the threshold voltage of theliquid crystal composition is satisfied. When preparing a liquid crystalcomposition for TFT or PSA, the content of component E is preferably 30%by weight or more, further preferably, 50% by weight or more, based onthe total weight of the composition. Moreover, when preparing a liquidcrystal composition for TN, STN or PSA, the content of component E ispreferably 30% by weight or more, further preferably, 40% by weight ormore, based on the total weight of the composition.

The liquid crystal composition of the invention preferably contains atleast one of compound (1) in a ratio of 0.1 to 99% by weight in order todevelop excellent characteristics.

The liquid crystal composition of the invention is generally preparedaccording to a publicly known method, for example, a method fordissolving necessary components under a high temperature. Moreover, anadditive well known to those skilled in the art is added according to anapplication, and thus a liquid crystal composition for a GH mode can beprepared to which an optically active compound or a polymerizablecompound, or a liquid crystal composition containing a polymerizationinitiator, or a dye as described later is added, for example. Theadditive is ordinarily well known to those skilled in the art, anddescribed in a literature or the like in detail.

The liquid crystal composition of the invention may further contain atleast one optically active compound. As the optically active compound, apublicly known chiral dopant is added. The chiral dopant is effective ininducing a helical structure of liquid crystals to adjust a requiredtwist angle, and preventing an inverted twist. Specific examples of thechiral dopants include optically active compounds represented byformulas (Op-1) to (Op-13).

A helical pitch of the liquid crystal composition of the invention canbe adjusted by adding the optically active compounds to the composition.The helical pitch is preferably adjusted in the range of 40 to 200micrometers for a liquid crystal composition for TFT and TN. The helicalpitch is preferably adjusted in the range of 6 to 20 micrometers for aliquid crystal composition for STN. Moreover, the helical pitch ispreferably adjusted in the range of 1.5 to 4 micrometers in a case of abistable TN mode. Moreover, two or more optically active compounds maybe added for the purpose of adjusting temperature dependence of thepitch.

The liquid crystal composition of the invention can also be used as aliquid crystal composition for the GH mode, if a dichroic dye such as amerocyanine, styryl, azo, azomethine, azoxy, quinophthalone,anthraquinone or tetrazine dye is added.

The liquid crystal composition of the invention can also be used as aliquid crystal composition for NCAP prepared by microencapsulatingnematic liquid crystals, a polymer dispersed liquid crystal displaydevice (PDLCD) prepared by forming a three-dimensional network polymerin liquid crystals, for example, a polymer network liquid crystaldisplay device (PNLCD), and a liquid crystal display device having anelectrically controlled birefringence (ECB) mode or DS mode.

Moreover, the liquid crystal composition of the invention can also beused as a liquid crystal composition for the polymer sustained alignment(PSA) mode by adding the polymerizable compound. Examples of thepolymerizable compound include a compound having a polymerizable groupsuch as acrylate, methacrylate, vinyl, vinyloxy, propenyl ether, epoxy,vinyl ketone and oxetane. The polymerizable compound is preferablypolymerized by irradiation with UV or the like under presence of asuitable initiator such as a photopolymerization initiator. Suitableconditions for polymerization, suitable types and suitable amounts ofinitiators are known to those skilled in the art and described in aliterature. For example, Irgacure 651 (registered tradename), Irgacure184 (registered tradename) or Darocure 1173 (registered tradename) (CibaJapan K. K.), each being the photopolymerization initiator, is suitablefor radical polymerization.

Method for Manufacturing a Liquid Crystal Composition

The liquid crystal composition concerning the invention can be prepared,for example, by mixing individual compounds when the compoundsconstituting each component are liquid, or by mixing individualcompounds and making the compounds liquid by heating and dissolution andthen shaking the compounds when the compounds contain a solid. Moreover,the liquid crystal composition concerning the invention can also beprepared by other publicly known methods.

Characteristics of a Liquid Crystal Composition

In the liquid crystal composition concerning the invention, the maximumtemperature of the nematic phase can be adjusted to 70° C. or higher,and the minimum temperature of the nematic phase to −20° C. or lower,and thus the temperature range of the nematic phase is wide.Accordingly, the liquid crystal display device including the liquidcrystal composition can be used in a wide temperature range.

In the liquid crystal composition concerning the invention, when thecomposition or the like is appropriately adjusted, the opticalanisotropy can be adjusted, for example, to the range of 0.10 to 0.13,or to the range of 0.05 to 0.18.

In the liquid crystal composition concerning the invention, a liquidcrystal composition having the dielectric anisotropy ordinarily in therange of −5.0 to −2.0, preferably, in the range of −4.5 to −2.5, can beobtained. A liquid crystal composition having the dielectric anisotropyin the range −4.5 to −2.5 can be suitably used as a liquid crystaldisplay device that operates according to the IPS mode, the VA mode orthe PSA mode.

Liquid Crystal Display Device

The liquid crystal composition concerning the invention can be used notonly for a liquid crystal display device that has an operating mode suchas the PC mode, the TN mode, the STN mode, the OCB mode or the PSA mode,and is driven according to an active matrix (AM) mode, but also for aliquid crystal display device that has an operating mode such as the PCmode, the TN mode, the STN mode, the OCB mode, the VA mode and the IPSmode, and is driven according to a passive matrix (PM) mode.

The liquid crystal display device according to the AM mode and the PMmode can be applied to any liquid crystal display of a reflective type,a transmissive type, a transflective type, or the like.

Moreover, the liquid crystal composition concerning the invention canalso be used for a dynamic scattering (DS) mode device using a liquidcrystal composition to which a conducting agent is added, a nematiccurvilinear aligned phase (NCAP) device prepared by microencapsulatingthe liquid crystal composition, or a polymer dispersed (PD) deviceprepared by forming a three-dimensional network polymer in the liquidcrystal composition, for example, a polymer network (PN) device.

Above all, the liquid crystal composition concerning the invention hasthe characteristics as described above. Therefore, the liquid crystalcomposition can be suitably used for a liquid crystal display deviceaccording to the AM mode to be driven by the operating mode using aliquid crystal composition having the negative dielectric anisotropy,such as the VA mode, the IPS mode or the PSA mode, particularlysuitably, a liquid crystal display device according to the AM mode to bedriven by the VA mode.

In the liquid crystal display device driven by the TN mode, the VA modeor the like, a direction of an electric field is perpendicular to adirection of a liquid crystal layer. On the other hand, in the liquidcrystal display device driven by the IPS mode or the like, the directionof the electric field is parallel to the direction of the liquid crystallayer. In addition, a structure of the liquid crystal display devicedriven by the VA mode is reported in K. Ohmuro, S. Kataoka, T. Sasakiand Y. Koike, SID'97 Digest of Technical Papers, 28, 845 (1997), and astructure of the liquid crystal display device driven by the IPS mode isreported in WO 91/10936 A (family: US5576867).

EXAMPLES Examples of Compound (1)

Hereinafter, the invention will be explained in more detail by way ofExamples, but the invention is not limited by the Examples. Unlessotherwise noted, “%” is expressed in terms of “% by weight.”

A compound obtained was identified using a spectrum obtained by ¹H NMRanalysis. Therefore, an analytical method will be first explained.

¹H NMR Analysis

As a measuring apparatus, DRX-500 (made by Bruker BioSpin Corporation)was used. A sample manufactured in Examples and so forth was dissolvedin a deuterated solvent such as CDCl₃ in which the sample was soluble,and measurement was carried out under the conditions of roomtemperature, 500 MHz and 32 times of accumulation. In the explanation ofthe nuclear magnetic resonance spectrum obtained, s, d, t, q, quin, sex,m and br stand for a singlet, a doublet, a triplet, a quartet, aquintet, a sextet, a multiplet and broad, respectively.Tetramethylsilane (TMS) was used for a reference material for a zeropoint of chemical shifts (6 values).

Measurement Sample

As a sample for determining values of physical properties of a liquidcrystal compound, two methods were applied: namely a case where thecompound per se was used as the sample, and a case where the compoundwas mixed with base liquid crystals to be used as the sample.

In the latter case where the sample prepared by mixing the liquidcrystal compound with the base liquid crystals was used, measurement wascarried out according to the method described below. First, a sample wasprepared by mixing 15% of a liquid crystal compound obtained and 85% ofbase liquid crystals. Then, extrapolated values were calculated, frommeasured values of the sample obtained, according to an extrapolationmethod shown in an equation as described below. The extrapolated valueswere described as values of physical properties of the compound.

(Extrapolated value)={100×(measured value of a sample)−(% of base liquidcrystals)×(measured value of the base liquid crystals)}/(% of liquidcrystal compound).  Equation

When a smectic phase or crystals precipitated at 25° C. even at theratio of the liquid crystal compound to the base liquid crystals asdescribed above, a ratio of the liquid crystal compound to the baseliquid crystals was changed in the order of (10%:90%), (5%:95%) and(1%:99%), and values of physical properties of the sample weredetermined at a ratio at which the smectic phase or the crystals did notprecipitate at 25° C.

As the base liquid crystals, base liquid crystals i was used when acompound having a positive dielectric anisotropy was used, and baseliquid crystals (ii) was used when a compound having a negativedielectric anisotropy was used. Compositions of base liquid crystals (i)and (ii) are as described below.

Base liquid crystals (i):

Base liquid crystals (ii):

Measuring Method

Values of physical properties were determined according to the methodsdescribed below. Most of the measuring methods are described in EIAJED-2521A of the Standard of Electronic Industries Association of Japan,or modified thereon. Moreover, no TFT was attached to a TN device or aVA device used for measurement.

Among measured values, values obtained using the liquid crystal compoundper se as the sample, and values obtained using the liquid crystalcomposition per se as the sample were described as were. In the case ofthe sample obtained by mixing the compound with the base liquidcrystals, values obtained according to the extrapolation method weredescribed.

Phase Structure and Phase Transition Temperature (° C.)

Measurement was carried out according to methods (1) and (2) asdescribed below.

(1) A sample was placed on a hot plate of a melting point apparatus(FP-52 Hot Stage made by Mettler-Toledo International Inc.) equippedwith a polarizing microscope, and a state of phase and a change thereofwere observed with the polarizing microscope while the sample was heatedat a rate of 3° C. per minute, and a kind of the phase was specified.

(2) A sample was heated and then cooled at a rate of 3° C. per minuteusing a differential scanning calorimeter, DSC-7 System or Diamond DSCSystem, made by PerkinElmer, Inc. A starting point (on set) of anendothermic peak or an exothermic peak caused by a phase change of thesample was determined by extrapolation, and thus a phase transitiontemperature was determined.

Hereinafter, the crystals were expressed as Cr, and when the crystalswere further distinguishable, each of the crystals was expressed as Cr₁or Cr₂. The smectic phase was expressed as Sm and a nematic phase as N.An isotropic liquid (isotropic) was expressed as Iso. When smectic Bphase or smectic A phase was distinguishable between the smectic phases,the phases were expressed as S_(B) or S_(A), respectively. As anexpression of the phase transition temperature, for example, “Cr 50.0 N100.0 Iso” shows that a phase transition temperature (CN) from thecrystals to the nematic phase is 50.0° C., and a phase transitiontemperature (NI) from the nematic phase to the isotropic liquid is100.0° C. A same rule was applied to other expressions.

Maximum Temperature of a Nematic Phase (T_(NI); ° C.)

A sample (a liquid crystal composition, or a mixture of a liquid crystalcompound and base liquid crystals) was placed on a hot plate of amelting point apparatus (FP-82 Hot Stage made by Mettler-ToledoInternational Inc.) equipped with a polarizing microscope, and wasobserved with the polarizing microscope while the sample was heated at arate of 1° C. per minute. Temperature when part of the sample changedfrom the nematic phase to the isotropic liquid was described as amaximum temperature of the nematic phase. Hereinafter, the maximumtemperature of the nematic phase may be occasionally abbreviated simplyas “maximum temperature.”

Compatibility at a Low Temperature

Samples were prepared in which base liquid crystals and a liquid crystalcompound were mixed to be 20%, 15%, 10%, 5%, 3% and 1% in an amount ofthe liquid crystal compound, and the samples were put in glass vials.The glass vials were put in freezers at −10° C. or −20° C. and kept fora fixed period of time, and then whether or not a domain of crystals ora smectic phase was generated was observed.

Viscosity (Bulk Viscosity; η; Measured at 20° C.; mPa·s)

A cone-plate (E type) rotational viscometer was used for measurement.

Viscosity (Rotational Viscosity; γ1; Measured at 25° C.; mPa·s)

Measurement was carried out according to a method described in M. Imaiet al., Molecular Crystals and Liquid Crystals, Vol. 259, 37 (1995). Asample (a liquid crystal composition, or a mixture of a liquid crystalcomposition and base liquid crystals) was put in a VA device in which adistance (cell gap) between two glass substrates was 20 micrometers.Voltage was stepwise applied to the device in the range of 30 V to 50 Vat an increment of 1 V. After a period of 0.2 second with no voltageapplication, application was repeated under conditions of only one ofrectangular waves (rectangular pulse; 0.2 second) and no application (2seconds). A peak current and a peak time of a transient currentgenerated by the application were measured. A value of rotationalviscosity was obtained from the measured values according to calculatingequation (8) on page 40 of the paper by Imai et al. In addition, a valueobtained by measuring dielectric anisotropy as described below was usedas the dielectric anisotropy necessary for the calculation.

Optical Anisotropy (Refractive Index Anisotropy; Measured at 25° C.; Δn)

Measurement was carried out by means of Abbe refractometer with apolarizing plate mounted on an ocular by using light at a wavelength of589 nanometers at a temperature of 25° C. A surface of a main prism wasrubbed in one direction, and then a sample (a liquid crystalcomposition, or a mixture of a liquid crystal compound and base liquidcrystals) was added dropwise onto the main prism. A refractive index(n∥) was measured when the direction of polarized light was parallel tothe direction of rubbing. A refractive index (n⊥) was measured when thedirection of polarized light was perpendicular to the direction ofrubbing. A value of optical anisotropy (Δn) was calculated from anequation: Δn=n∥−n⊥.

Dielectric Anisotropy (Δ∈; Measured at 25° C.)

Dielectric anisotropy was measured according to a method as describedbelow.

An ethanol (20 mL) solution of octadecyl triethoxysilane (0.16 mL) wasapplied to a well-washed glass substrate. After rotating the glasssubstrate with a spinner, the glass substrate was heated at 150° C. for1 hour. A VA device in which a distance (cell gap) between two glasssubstrates was 20 micrometers was assembled.

In a similar manner, a polyimide alignment film was formed on the glasssubstrate. After rubbing treatment was applied to the alignment filmobtained on the glass substrate, a TN device in which a distance (cellgap) between two glass substrates was 9 micrometers and a twist anglewas 80 degrees was assembled.

A sample (a liquid crystal composition, or a mixture of a liquid crystalcompound and base liquid crystals) was put in the VA device obtained, avoltage of 0.5 V (1 kHz, sine waves) was applied to the device, and adielectric constant (∈∥) in the major axis direction of liquid crystalmolecules was measured.

Moreover, a sample (a liquid crystal composition, or a mixture of aliquid crystal compound and base liquid crystals) was put in the TNdevice obtained, a voltage of 0.5 V (1 kHz, sine waves) was applied tothe device, and a dielectric constant (∈⊥) in the minor axis directionof the liquid crystal molecules was measured. A value of dielectricanisotropy was calculated from an equation: Δ∈=∈∥−∈⊥.

Voltage Holding Ratio (VHR; Measured at 25° C.; %)

A TN device used for measurement had a polyimide alignment film, and adistance (cell gap) between two glass substrates was 6 micrometers. Asample (a liquid crystal composition, or a mixture of a liquid crystalcompound and base liquid crystals) was put in the device, and then thedevice was sealed with an ultraviolet-polymerizable adhesive. A pulsevoltage (60 microseconds at 5 V) was applied to the TN device and thedevice was charged. A decaying voltage was measured for 16.7milliseconds with a high-speed voltmeter, and area A between a voltagecurve and a horizontal axis in a unit cycle was determined. Area B is anarea without decay. A voltage holding ratio was expressed in terms of apercentage of area A to area B.

Elastic Constant (K₁₁, K₃₃; Measured at 25° C.)

Elastic Constant Measurement System Model EC-1 made by TOYO Corporationwas used for measurement. A sample was put in a vertical alignment cellin which a distance (cell gap) between two glass substrates was 20micrometers. An electric charge from 20 V to 0 V was applied to thecell, and electrostatic capacity and applied voltage were measured.Measured values of the electrostatic capacity (C) and the appliedvoltage (V) were fitted to equation (2.98) and equation (2.101) on page75 of “Liquid Crystal Device Handbook” (Ekisho Debaisu Handobukku inJapanese) (The Nikkan Kogyo Shimbun, Ltd.) and a value of elasticconstant was obtained from equation (2.100).

Example 1 Synthesis of6-(trans-4-propylcyclohexyl)-3-(trans-4-pentylcyclohexyl)methoxy-3-cyclohexene(compound(1-3-1-18))

First Step Under a nitrogen atmosphere, 2.4 g of4-(trans-4-propylcyclohexyl)-2-cyclohexene-1-ol (r-1) was dissolved into50 mL of THF, 0.52 g of 60% sodium hydride was added under ice-cooling,and the resultant mixture was stirred at room temperature for 1 hour.Thereto, 2.3 g of potassium iodide and 3.2 g of(trans-4-pentylcyclohexyl)bromomethane (r-2) dissolved in 30 mL of THFwere added, and the resultant mixture was stirred under heating refluxfor 8 hours. The resultant reaction mixture was poured into water, andsubjected to extraction with toluene. Combined organic layers werewashed with saturated brine, and then dried over anhydrous magnesiumsulfate. A solvent was evaporated under reduced pressure, and a residuewas purified by silica gel column chromatography(eluate:heptane:toluene=1:1 (in a volume ratio)), and further purifiedby recrystallization from a mixed solvent of heptane: Solmix A-11(registered tradename; Japan Alcohol Trading Co., Ltd.)=1:2 (in a volumeratio), and thus 0.15 g of6-(trans-4-propylcyclohexyl)-3-(trans-4-pentylcyclohexyl)methoxycyclohexene [compound (1-3-1-18) was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 5.73 (dd, 2H), 3.87-3.83 (m, 1H), 3.33-3.25 (m,2H), 2.10-2.08 (m, 1H), 2.02-1.98 (m, 1H), 1.83-1.63 (m, 10H), 1.51-1.41(m, 2H), 1.35-1.15 (m, 16H), 1.03 (m, 2H), 0.96-0.83 (t, 13H).

As a transition temperature, an intrinsic value of the compound wasdescribed. Values of physical properties of compound (1-3-1-18) were asdescribed below.

Transition temperature: Cr 16.2 SmB 127 Iso.

Example 2 Synthesis of3-(4-(trans-4-butylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound(1-2-1-4))

First Step

Under a nitrogen atmosphere, 3.0 g of4-(4-(trans-4-butylcyclohexyl)cyclohexyl)-2-cyclohexenone (r-3) wasdissolved into 50 mL of THF, 11.4 mL of pentylmagnesium bromide THFsolution (1 M/L) was added dropwise thereto, and the resultant mixturewas stirred at 50° C. for 30 minutes, and then stirred at roomtemperature overnight. A saturated aqueous solution of ammonium chloridewas added dropwise under ice-cooling, the resultant mixture wassubjected to extraction with ethyl acetate, and then organic layers werecombined, the resultant organic layer was washed with saturated brine,and then dried over anhydrous magnesium sulfate. A solvent wasevaporated under reduced pressure, and the resultant residue waspurified by fractionation on silica gel column chromatography(eluate:heptane:ethyl acetate=7:3 (in a volume ratio)), and thus 2.68 gof 4-(4-(trans-4-butylcyclohexyl)cyclohexyl)-1-pentyl-2-cyclohexene-1-ol(compound (r-4)) was obtained.

Second Step

Under a nitrogen atmosphere, 2.68 g of compound (r-4) was dissolved intoa mixed solvent of 70 mL of dichloromethane and 70 mL of acetonitrile,and 1.65 g of triethylsilane was added thereto, and then 12.3 g of atrifluoroborane-diethyl ether complex was added dropwise at −50° C., theresultant mixture was stirred at −78° C. for 30 minutes, and thenstirred at room temperature for 1 hour. A saturated aqueous solution ofsodium hydrogencarbonate was added dropwise to terminate a reaction, theresultant mixture was subjected to extraction with dichloromethane, andthen organic layers were combined, the resultant organic layer waswashed with a saturated aqueous solution of sodium hydrogencarbonate andsaturated brine, and then dried over anhydrous magnesium sulfate. Asolvent was evaporated under reduced pressure, and the resultant residuewas purified by fractionation on silica gel column chromatography(eluate:heptane), and further purified by recrystallization from a mixedsolvent of heptane: Solmix A-11 (registered tradename; Japan AlcoholTrading Co., Ltd.)=1:2 (in a volume ratio), and dried, and thus 1.11 gof 3-(4-(trans-4-butylcyclohexyl)cyclohexyl)-6-pentylcyclohexene(compound (1-2-1-4)) was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 5.58 (dd, 1H), 5.39 (d, 1H), 2.45-1.92 (m, 6H),1.83-1.71 (m, 10H), 1.41-1.14 (m, 10H), 1.00-0.85 (m, 20H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (i) weredescribed. Values of physical properties of compound (1-2-1-4) were asdescribed below.

Transition temperature: Cr 14.4 SmB 218.4 Iso.

T_(NI)=159.7° C., Δ∈=0.40, Δn=0.077.

Example 3 Synthesis of3-(4-(trans-4-propylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound(1-2-1-1))

First Step

Under a nitrogen atmosphere, 4.0 g of4-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-2-cyclohexenone (r-4) wasdissolved into 50 mL of THF, 15.8 mL of pentylmagnesium bromide THFsolution (1 M/L) was added dropwise thereto at room temperature, and theresultant mixture was stirred at 50° C. for 30 minutes, and then stirredat room temperature overnight. A saturated aqueous solution of ammoniumchloride was added dropwise thereto under ice-cooling, the resultantmixture was subjected to extraction with ethyl acetate, and then organiclayers were combined, the resultant organic layer was washed withsaturated brine, and then dried over anhydrous magnesium sulfate. Asolvent was evaporated under reduced pressure, and the resultant residuewas purified by fractionation on silica gel column chromatography(eluate:heptane:ethyl acetate=7:3 (in a volume ratio)), and thus 3.95 gof 4-(4-(trans-4-butylcyclohexyl)cyclohexyl)-1-pentyl-2-cyclohexene-1-01(compound (r-6)) was obtained.

Second Step

Under a nitrogen atmosphere, 3.95 g of compound (r-6) was dissolved intoa mixed solvent of 70 mL of dichloromethane and 70 mL of acetonitrile,1.83 g of triethylsilane was added thereto, and then 1.94 g of atrifluoroborane-diethyl ether complex was added dropwise at −50° C., theresultant mixture was stirred at −78° C. for 30 minutes, and thenstirred at room temperature for 1 hour. A saturated aqueous solution ofsodium hydrogencarbonate was added dropwise to terminate a reaction, theresultant mixture was subjected to extraction with dichloromethane, andthen organic layers were combined, the resultant organic layer waswashed with a saturated aqueous solution of sodium hydrogencarbonate andsaturated brine, and then dried over anhydrous magnesium sulfate. Asolvent was evaporated under reduced pressure, and the resultant residuewas purified by fractionation on silica gel column chromatography(eluate:heptane), and further purified by recrystallization from ethylacetate, and dried, and thus 1.44 g of3-(4-(trans-4-propylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound(1-2-1-1)) was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 5.56 (dd, 1H), 5.39 (d, 1H), 2.05-1.92 (m, 6H),1.86-1.71 (m, 10H), 1.43-1.11 (m, 10H), 1.06-0.85 (m, 18H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(ΔE) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (i) weredescribed. Values of physical properties of compound (1-2-1-1) were asdescribed below.

Transition temperature: Cr 16.1 SmB 214.6 Iso.

T_(NI)=167.7° C., Δ∈=−0.30, Δn=0.077.

Example 4 Synthesis of3-(4-(trans-4-ethylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound(1-2-1-6))

First Step

Under a nitrogen atmosphere, 4.0 g of4-(4-(trans-4-ethylcyclohexyl)cyclohexyl)-2-cyclohexenone (r-7) wasdissolved into 50 mL of THF, 16.8 mL of pentylmagnesium bromide THFsolution (1 M/L) was added dropwise thereto at room temperature, and theresultant mixture was stirred at 50° C. for 30 minutes, and then stirredat room temperature overnight. A saturated aqueous solution of ammoniumchloride was added dropwise under ice-cooling, the resultant mixture wassubjected to extraction with ethyl acetate, and then organic layers werecombined, the resultant organic layer was washed with saturated brine,and then dried over anhydrous magnesium sulfate. A solvent wasevaporated under reduced pressure, and the resultant residue waspurified by fractionation on silica gel column chromatography(eluate:heptane:ethyl acetate=7:3 (in a volume ratio)), and thus 3.83 gof 4-(4-(trans-4-ethylcyclohexyl)cyclohexyl)-1-pentyl-2-cyclohexene-1-01(compound (r-6)) was obtained.

Second Step

Under a nitrogen atmosphere, 3.83 g of compound (r-8) was dissolved intoa mixed solvent of 70 mL of dichloromethane and 70 mL of acetonitrile,1.85 g of triethylsilane was added thereto, and then 1.80 g oftrifluoroborane-diethyl ether complex was added dropwise at −50° C., theresultant mixture was stirred at −78° C. for 30 minutes, and thenstirred at room temperature for 1 hour. A saturated aqueous solution ofsodium hydrogencarbonate was added dropwise to terminate a reaction, theresultant mixture was subjected to extraction with dichloromethane, andthen organic layers were combined, the resultant organic layer waswashed with a saturated aqueous solution of sodium hydrogencarbonate andsaturated brine, and then dried over anhydrous magnesium sulfate. Asolvent was evaporated under reduced pressure, and the resultant residuewas purified by fractionation on silica gel column chromatography(eluate:heptane), and further purified by recrystallization from ethylacetate, and dried, and thus 1.40 g of3-(4-(trans-4-ethylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound(1-2-1-6)) was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 5.55 (dd, 1H), 5.36 (d, 1H), 2.05-1.92 (m, 6H),1.86-1.71 (m, 10H), 1.43-1.11 (m, 10H), 1.06-0.85 (m, 16H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (i) weredescribed. Values of physical properties of compound (1-2-1-6) were asdescribed below.

Transition temperature: Cr −14.3 SmB 194.5 Iso.

T_(NI)=145.7° C., Δ∈=−0.37, Δn=0.064.

Example 5 Synthesis of3-(4-(trans-4-propylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound(1-2-1-10))

First Step

Under a nitrogen atmosphere, 4.0 g of4-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-2-cyclohexenone (r-9) wasdissolved into 50 mL of THF, 14.5 mL of butylmagnesium bromide THFsolution (1 M/L) was added dropwise thereto at room temperature, and theresultant mixture was stirred at 50° C. for 30 minutes, and then stirredat room temperature overnight. A saturated aqueous solution of ammoniumchloride was added dropwise under ice-cooling, the resultant mixture wassubjected to extraction with ethyl acetate, and then organic layers werecombined, the resultant organic layer was washed with saturated brine,and then dried over anhydrous magnesium sulfate. A solvent wasevaporated under reduced pressure, and the resultant residue waspurified by fractionation on silica gel column chromatography(eluate:heptane:ethyl acetate=7:3 (in a volume ratio)), and thus 4.70 gof 4-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-1-butyl-2-cyclohexene-1-ol(compound (r-10)) was obtained.

Second Step

Under a nitrogen atmosphere, 4.70 g of compound (r-10) was dissolvedinto a mixed solvent of 70 mL of dichloromethane and 70 mL ofacetonitrile, 2.11 g of triethylsilane was added thereto, and then 2.06g of trifluoroborane-diethyl ether complex was added dropwise at −50°C., the resultant mixture was stirred at −78° C. for 30 minutes, andthen stirred at room temperature for 1 hour. A saturated aqueoussolution of sodium hydrogencarbonate was added dropwise to terminate areaction, the resultant mixture was subjected to extraction withdichloromethane, and then organic layers were combined, the resultantorganic layer was washed with a saturated aqueous solution of sodiumhydrogencarbonate and saturated brine, and then dried over anhydrousmagnesium sulfate. A solvent was evaporated under reduced pressure, andthe resultant residue was purified by fractionation on silica gel columnchromatography (eluate:heptane), and further purified byrecrystallization from ethyl acetate, and dried, and thus 2.04 g of3-(4-(trans-4-pentylcyclohexyl)cyclohexyl)-6-butylcyclohexene (compound(1-2-1-10)) was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 5.55 (dd, 1H), 5.36 (d, 1H), 2.02-1.90 (m, 6H),1.83-1.68 (m, 10H), 1.37-1.08 (m, 10H), 1.03-0.79 (m, 20H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(ΔE) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (i) weredescribed. Values of physical properties of compound (1-2-1-10) were asdescribed below.

Transition temperature: Cr 7.6 SmB 223.4 Iso.

T_(NI)=160.7° C., Δ∈=1.80, Δn=0.067.

Example 6 Synthesis of 3-(trans-4-propylcyclohexyl)-6-pentylcyclohexene(compound (1-1-1-3))

First Step

Under a nitrogen atmosphere, 5.0 g of4-(trans-4-propylcyclohexyl)-2-cyclohexenone (r-11) was dissolved into50 mL of THF, 27.2 mL of pentylmagnesium bromide THF solution (1 M/L)was added dropwise thereto at room temperature, and the resultantmixture was stirred at 50° C. for 30 minutes, and then stirred at roomtemperature overnight. A saturated aqueous solution of ammonium chloridewas added dropwise under ice-cooling, the resultant mixture wassubjected to extraction with ethyl acetate, and then organic layers werecombined, the resultant organic layer was washed with saturated brine,and then dried over anhydrous magnesium sulfate. A solvent wasevaporated under reduced pressure, and the resultant residue waspurified by fractionation on silica gel column chromatography(eluate:heptane:ethyl acetate=7:3), and thus 6.56 g of4-(4-(trans-4-butylcyclohexyl)cyclohexyl)-1-pentyl-2-cyclohexene-1-ol(compound (r-12)) was obtained.

Second Step

Under a nitrogen atmosphere, 6.56 g of compound (r-12) was dissolvedinto a mixed solvent of 100 mL of dichloromethane and 100 mL ofacetonitrile, 3.91 g of triethylsilane was added thereto, and then 4.13g of trifluoroborane-diethyl ether complex was added dropwise at −50°C., the resultant mixture was stirred at −78° C. for 30 minutes, andthen stirred at room temperature for 1 hour. A saturated aqueoussolution of sodium hydrogencarbonate was added dropwise to terminate areaction, the resultant mixture was subjected to extraction withdichloromethane, and then organic layers were combined, the resultantorganic layer was washed with a saturated aqueous solution of sodiumhydrogencarbonate and saturated brine, and then dried over anhydrousmagnesium sulfate. A solvent was evaporated under reduced pressure, andthe resultant residue was purified by fractionation on silica gel columnchromatography (eluate:heptane), and further purified byrecrystallization from ethyl acetate, and dried, and thus 1.11 g of3-(4-(trans-4-propylcyclohexyl)-6-pentylcyclohexene (compound (1-1-1-3))was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 5.59 (dd, 1H), 5.39 (d, 1H), 2.45-1.92 (m, 4H),1.82-1.74 (m, 6H), 1.43-1.14 (m, 8H), 1.12-1.06 (m, 2H), 1.04-0.97 (m,2H), 0.95-0.85 (m, 12H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (i) weredescribed. Values of physical properties of compound (1-1-1-3) were asdescribed below.

Transition temperature: Cr −13.0 SmB 26.7 Iso.

T_(NI)=13.0° C., Δ∈=−2.03, Δn=0.024.

Example 7 Synthesis of3-(trans-4-(4-methoxyphenyl)cyclohexyl)-6-pentylcyclohexene (compound(1-2-3-2))

First Step

Under a nitrogen atmosphere, 4.00 g of4-(trans-4-(methoxyphenyl)cyclohexyl)-2-cyclohexenone (r-13) wasdissolved into 60 mL of THF, 17.0 mL of pentylmagnesium bromide THFsolution (1 M/L) was added dropwise thereto at room temperature, and theresultant mixture was stirred at 50° C. for 30 minutes, and then stirredat room temperature overnight. A saturated aqueous solution of ammoniumchloride was added dropwise under ice-cooling, the resultant mixture wassubjected to extraction with ethyl acetate, and then organic layers werecombined, the resultant organic layer was washed with saturated brine,and then dried over anhydrous magnesium sulfate. A solvent wasevaporated under reduced pressure, and the resultant residue waspurified by fractionation on silica gel column chromatography(eluate:heptane:ethyl acetate=7:3), and thus 4.73 g of4-(trans-4-(4-methoxyphenyl)cyclohexyl)-1-pentyl-2-cyclohexene-1-ol(compound (r-14)) was obtained.

Second Step

Under a nitrogen atmosphere, 4.73 g of compound (r-14) was dissolvedinto a mixed solvent of 80 mL of dichloromethane and 80 mL ofacetonitrile, 2.47 g of triethylsilane was added thereto, and then 2.60g of trifluoroborane-diethyl ether complex was added dropwise at −50°C., the resultant mixture was stirred at −78° C. for 30 minutes, andthen stirred at room temperature for 1 hour. A saturated aqueoussolution of sodium hydrogencarbonate was added dropwise to terminate areaction, the resultant mixture was subjected to extraction withdichloromethane, and then organic layers were combined, the resultantorganic layer was washed with a saturated aqueous solution of sodiumhydrogencarbonate and saturated brine, and then dried over anhydrousmagnesium sulfate. A solvent was evaporated under reduced pressure, andthe resultant residue was purified by fractionation on silica gel columnchromatography (eluate:heptane:toluene=1:1), and further purified byrecrystallization from heptane: Solmix=1:2), and dried, and thus 0.94 gof3-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-6-propylcyclohexene(compound (1-2-3-2)) was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 7.13 (d, 2H), 6.83 (d, 2H), 5.59 (dd, 1H), 5.39(d, 1H), 3.78 (s, 3H), 2.41 (tt, 1H), 2.07-1.76 (m, 10H), 1.45-1.09 (m,13H), 0.89 (t, 3H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (i) weredescribed. Values of physical properties of compound (1-2-3-2) were asdescribed below.

Transition temperature: Cr 53.8 SmB 79.8 N 143.7 Iso.

T_(NI)=134.4° C., Δ∈=3.90, Δn=0.117.

Example 8 Synthesis of3-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-6-propylcyclohexene(compound (1-2-3-25))

First Step

Under a nitrogen atmosphere, 4.97 g of4-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-2-cyclohex enone(r-15) was dissolved into 60 mL of THF, 18.0 mL of propylmagnesiumbromide THF solution (1 M/L) was added dropwise thereto at roomtemperature, and the resultant mixture was stirred at 50° C. for 30minutes, and then stirred at room temperature overnight. A saturatedaqueous solution of ammonium chloride was added dropwise underice-cooling, the resultant mixture was subjected to extraction withethyl acetate, and then organic layers were combined, the resultantorganic layer was washed with saturated brine, and then dried overanhydrous magnesium sulfate. A solvent was evaporated under reducedpressure, and the resultant residue was purified by fractionation onsilica gel column chromatography (eluate:heptane:ethyl acetate=6:4), andthus 3.79 g of4-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-1-propyl-2-cyclohexene-1-ol(compound (r-16)) was obtained.

Second Step

Under a nitrogen atmosphere, 3.79 g of compound (r-16) was dissolvedinto a mixed solvent of 70 mL of dichloromethane and 70 mL ofacetonitrile, 1.79 g of triethylsilane was added thereto, and then 1.84g of trifluoroborane-diethyl ether complex was added dropwise at −50°C., the resultant mixture was stirred at −78° C. for 30 minutes, andthen stirred at room temperature for 1 hour. A saturated aqueoussolution of sodium hydrogencarbonate was added dropwise to terminate areaction, the resultant mixture was subjected to extraction withdichloromethane, and then organic layers were combined, the resultantorganic layer was washed with a saturated aqueous solution of sodiumhydrogencarbonate and saturated brine, and then dried over anhydrousmagnesium sulfate. A solvent was evaporated under reduced pressure, andthe resultant residue was purified by fractionation on silica gel columnchromatography (eluate:heptane:toluene=7:3), and further purified byrecrystallization from heptane: Solmix=1:2), and dried, and thus 1.25 gof 3-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-6-propylcyclohexane (compound (1-2-3-25)) wasobtained.

¹H-NMR (CDCl₃ δ (ppm)); 6.86 (m, 1H), 6.69 (m, 1H), 5.61 (dd, 1H), 5.41(d, 1H), 4.11 (q, 2H), 2.76 (tt, 1H), 2.15-1.78 (m, 10H), 1.45 (t, 3H),1.43-1.14 (m, 9H), 0.90 (t, 3H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (ii) weredescribed. Values of physical properties of compound (1-2-3-25) were asdescribed below.

Transition temperature: Cr 67.4 N 129.1 Iso.

T_(NI)=115.3° C., Δ∈=−5.89, Δn=0.112.

Example 9 Synthesis of3-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-6-pentylcyclohexene(compound (1-2-3-26))

First Step

Under a nitrogen atmosphere, 4.00 g of4-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-2-cyclohex enone(r-15) was dissolved into 60 mL of THF, 14.4 mL of pentylmagnesiumbromide THF solution (1 M/L) was added dropwise thereto at roomtemperature, and the resultant mixture was stirred at 50° C. for 30minutes, and then stirred at room temperature overnight. A saturatedaqueous solution of ammonium chloride was added dropwise underice-cooling, the resultant mixture was subjected to extraction withethyl acetate, and then organic layers were combined, the resultantorganic layer was washed with saturated brine, and then dried overanhydrous magnesium sulfate. A solvent was evaporated under reducedpressure, and the resultant residue was purified by fractionation onsilica gel column chromatography (eluate:heptane:ethyl acetate=6:4), andthus 3.45 g of4-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-1-pentyl-2-cyclohexene-1-ol(compound (r-17)) was obtained.

Second Step

Under a nitrogen atmosphere, 3.45 g of compound (r-17) was dissolvedinto a mixed solvent of 70 mL of dichloromethane and 70 mL ofacetonitrile, 1.50 g of triethylsilane was added thereto, and then 1.57g of trifluoroborane-diethyl ether complex was added dropwise at −50°C., the resultant mixture was stirred at −78° C. for 30 minutes, andthen stirred at room temperature for 1 hour. A saturated aqueoussolution of sodium hydrogencarbonate was added dropwise to terminate areaction, the resultant mixture was subjected to extraction withdichloromethane, and then organic layers were combined, the resultantorganic layer was washed with a saturated aqueous solution of sodiumhydrogencarbonate and saturated brine, and then dried over anhydrousmagnesium sulfate. A solvent was evaporated under reduced pressure, andthe resultant residue was purified by fractionation on silica gel columnchromatography (eluate:heptane:toluene=7:3), and further purified byrecrystallization from heptane: Solmix=1:2), and dried, and thus 1.12 gof3-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-6-pentylcyclohexane(compound (1-2-3-26)) was obtained.

¹H-NMR (CDCl₃δ (ppm)); 6.83 (m, 1H), 6.66 (m, 1H), 5.59 (dd, 1H), 5.38(d, 1H), 4.08 (q, 2H), 2.74 (tt, 1H), 2.06-1.76 (m, 10H), 1.44 (t, 3H),1.47-1.11 (m, 13H), 0.90 (t, 3H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (ii) weredescribed. Values of physical properties of compound (1-2-3-26) were asdescribed below.

Transition temperature: Cr 52.2 N 126.5 Iso.

T_(NI)=113.3° C., Δ∈=−5.60, Δn=0.105.

Example 10 Synthesis of3-(trans-4-((2,3-difluoro-4-ethyloxyphenyloxy)methyl)cyclohexyl)-6-propylcyclohexene(compound (1-2-3-41))

First Step

Under a nitrogen atmosphere, 4.0 g of3-(trans-4-((2,3-difluoro-4-ethyloxyphenyloxy)methyl)cyclohexyl)-2-cyclohexenone(r-17) was dissolved into 60 mL of THF, 13.0 mL of propylmagnesiumbromide THF solution (1 M/L) was added dropwise thereto at roomtemperature, and the resultant mixture was stirred at 50° C. for 30minutes, and then stirred at room temperature overnight. A saturatedaqueous solution of ammonium chloride was added dropwise underice-cooling, the resultant mixture was subjected to extraction withethyl acetate, and then organic layers were combined, the resultantorganic layer was washed with saturated brine, and then dried overanhydrous magnesium sulfate. A solvent was evaporated under reducedpressure, and the resultant residue was purified by fractionation onsilica gel column chromatography (eluate:heptane:ethyl acetate=6:4), andthus 3.16 g of3-(trans-4-((2,3-difluoro-4-ethyloxyphenyloxy)methyl)cyclohexyl)-6-propyl-6-hydroxycyclohexene(compound (r-18)) was obtained.

Second Step

Under a nitrogen atmosphere, 3.16 g of compound (r-18) was dissolvedinto a mixed solvent of 70 mL of dichloromethane and 70 mL ofacetonitrile, 1.35 g of triethylsilane was added thereto, and then 1.42g of trifluoroborane-diethyl ether complex was added dropwise at −50°C., the resultant mixture was stirred at −78° C. for 30 minutes, andthen stirred at room temperature for 1 hour. A saturated aqueoussolution of sodium hydrogencarbonate was added dropwise to terminate areaction, the resultant mixture was subjected to extraction withdichloromethane, and then organic layers were combined, the resultantorganic layer was washed with a saturated aqueous solution of sodiumhydrogencarbonate and saturated brine, and then dried over anhydrousmagnesium sulfate. A solvent was evaporated under reduced pressure, andthe resultant residue was purified by fractionation on silica gel columnchromatography (eluate:heptane:toluene=6:4), and further purified byrecrystallization from heptane: Solmix=1:4), and dried, and thus 1.09 gof3-(trans-4-((2,3-difluoro-4-ethyloxyphenyloxy)methyl)cyclohexyl)-6-propylcyclohexene(compound (1-2-3-41)) was obtained.

¹H-NMR (CDCl₃, δ (ppm)); 6.63 (m, 2H), 5.59 (dd, 1H), 5.39 (d, 1H), 4.07(q, 2H), 3.79 (d, 2H), 2.07-1.76 (m, 11H), 1.42 (t, 3H), 1.41-1.04 (m,9H), 0.90 (t, 3H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (ii) weredescribed. Values of physical properties of compound (1-2-3-41) were asdescribed below.

Transition temperature: Cr 46.1 N 108.1 Iso.

T_(NI)=103.9° C., Δ∈=−7.49, Δn=0.105.

Example 11 Synthesis of3-(trans-4-((2,3-difluoro-4-ethoxyphenyloxy)methyl)cyclohexyl)-6-pentylcyclohexene(compound (1-2-3-42))

First Step

Under a nitrogen atmosphere, 4.00 g of3-(trans-4-((2,3-difluoro-4-ethyloxyphenyloxy)methyl)cyclohexyl)-2-cyclohexenone(r-17) was dissolved into 60 mL of THF, 13.2 mL of pentylmagnesiumbromide THF solution (1 M/L) was added dropwise thereto at roomtemperature, and the resultant mixture was stirred at 50° C. for 30minutes, and then stirred at room temperature overnight. A saturatedaqueous solution of ammonium chloride was added dropwise underice-cooling, the resultant mixture was subjected to extraction withethyl acetate, and then organic layers were combined, the resultantorganic layer was washed with saturated brine, and then dried overanhydrous magnesium sulfate. A solvent was evaporated under reducedpressure, and the resultant residue was purified by fractionation onsilica gel column chromatography (eluate:heptane:ethyl acetate=6:4), andthus 1.99 g of3-(trans-4-((2,3-difluoro-4-ethyloxyphenyloxy)methyl)cyclohexyl)-6-pentyl-6-hydroxycyclohexene(compound (r-19)) was obtained.

Second Step

Under a nitrogen atmosphere, 1.99 g of compound (r-19) was dissolvedinto a mixed solvent of 70 mL of dichloromethane and 70 mL ofacetonitrile, 0.80 g of triethylsilane was added thereto, and then 0.84g of trifluoroborane-diethyl ether complex was added dropwise at −50°C., the resultant mixture was stirred at −78° C. for 30 minutes, andthen stirred at room temperature for 1 hour. A saturated aqueoussolution of sodium hydrogencarbonate was added dropwise to terminate areaction, the resultant mixture was subjected to extraction withdichloromethane, and then organic layers were combined, the resultantorganic layer was washed with a saturated aqueous solution of sodiumhydrogencarbonate and saturated brine, and then dried over anhydrousmagnesium sulfate. A solvent was evaporated under reduced pressure, andthe resultant residue was purified by fractionation on silica gel columnchromatography (eluate:heptane:toluene=7:3), and further purified byrecrystallization from heptane: Solmix=1:4), and dried, and thus 0.45 gof3-(trans-4-((2,3-difluoro-4-ethoxyphenyloxy)methyl)cyclohexyl)-6-pentylcyclohexene(compound (1-2-3-42)) was obtained.

¹H-NMR (CDCl₃ δ (ppm)); 6.60 (m, 2H), 5.57 (dd, 1H), 5.37 (d, 1H), 4.05(q, 2H), 3.76 (d, 2H), 2.07-1.76 (m, 11H), 1.42 (t, 3H), 1.41-1.04 (m,13H), 0.90 (t, 3H).

As a transition temperature, an intrinsic value of the compound wasdescribed, and as a maximum temperature (T_(NI)), dielectric anisotropy(Δ∈) and optical anisotropy (Δn), extrapolated values convertedaccording to the extrapolation method from measured values of the sampleprepared by mixing the compound with base liquid crystals (ii) weredescribed. Values of physical properties of compound (1-2-3-42) were asdescribed below.

Transition temperature: Cr₁ 29.2 Cr₂ 32.1 N 107.2 Iso.

T_(NI)=99.3° C., Δ∈=−7.46, Δn=0.102.

Comparative Example 1 Compatibility at a Low Temperature

As a comparative compound,

trans-4-(trans-4-(trans-4-butylcyclohexyl)cyclohexyl)-pentylcyclohexane(Ex-1) being compound 25 disclosed in JP H9-110734 A was prepared.

Then, five compounds described above were mixed and base liquid crystalsi having a nematic phase was prepared. Physical properties of the baseliquid crystals i were as described below.

Maximumtemperature (T_(NI))=71.7° C.; viscosity (η₂₀)=27.0 mPa·s;optical anisotropy (Δn)=0.137; dielectric anisotropy (Δ∈)=11.

Compatibility of compound (Ex-1) at a low temperature was measured byusing the base liquid crystals i and cooling a mixture at −20° C. for 30days. As a result, crystals precipitated and the nematic phase was notmaintained at a concentration of 1% or more.

Compatibility of Compound (1-2-1-10) at a Low Temperature

Compatibility, at a low temperature, of3-(4-(trans-4-propylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound1-2-1-10) obtained in Example 5 was measured by using base liquidcrystals i and cooling a mixture at −20° C. for 30 days. As a result,the nematic phase was maintained at a concentration of 5% or less.

The findings show that compound (1-2-1-10) is superior to comparativecompound (Ex-1) in solubility in base liquid crystals at a lowtemperature, and useful as a liquid crystal compound.

Comparative Example 2 Compatibility at a Low Temperature

As a comparative compound,

trans-4-(trans-4-(trans-4-ethylcyclohexyl)cyclohexyl)-pentylcyclohexane(Ex-2) being compound 12 disclosed in JP H9-110734 A was prepared.

In a manner similar to Comparative Example 1, compatibility of compound(Ex-2) at a low temperature was measured by using the base liquidcrystals i and cooling a mixture at −20° C. for 30 days. As a result,crystals precipitated after 8 days and the nematic phase was notmaintained even at a concentration of 1%.

Compatibility of Compound (1-2-1-6) at a Low Temperature

Compatibility, at a low temperature, of3-(4-(trans-4-ethylcyclohexyl)cyclohexyl)-6-pentylcyclohexene (compound1-2-1-6) obtained in Example 4 was measured by using base liquidcrystals i and cooling a mixture at −20° C. for 30 days. As a result,the nematic phase was maintained at a concentration of 5% or less.

The findings show that compound (1-2-1-6) is superior to comparativecompound (Ex-2) in solubility in base liquid crystals at a lowtemperature, and useful as a liquid crystal compound.

Comparative Example 3 Compatibility at a Low Temperature

As a comparative compound,trans-4-propyl-trans-4′-(2,3-difluoroethoxyphenyl)-1,1′-bicyclohexyl(Ex-3) was prepared.

Chemical shifts (δ (ppm)) by ¹H NMR analysis were as described below,and the compound obtained was identified to betrans-4-propyl-trans-4′-(2,3-difluoroethoxyphenyl)-1,1′-bicycloh exyl(Ex-1). ¹H-NMR (CDCl₃, δ (ppm)); 6.82 (dd, 1H), 6.64 (dd, 1H), 4.06 (q,2H), 2.71 (tt, 1H), 1.89-1.79 (m, 4H), 1.79-1.69 (m, 4H), 1.45-1.26 (m,14H), 1.20-1.04 (m, 4H), 0.90-0.79 (t, 3H).

A transition temperature of compound (Ex-1) was as described below.

Transition temperature: C 66.9 S_(B) 79.9 N 185.1 Iso.

Then, five compounds described above were mixed and base liquid crystals(ii) having a nematic phase was prepared. Physical properties of thebase liquid crystals (ii) were as described below.

Maximumtemperature (T_(NI))=74.6° C.; viscosity (η₂₀)=18.9 mPa·s;optical anisotropy (Δn)=0.087; dielectric anisotropy (Δ∈)=−1.3.

Compatibility of compound (Ex-1) at a low temperature was measured byusing the base liquid crystals (ii) and cooling a mixture at −10° C. for30 days. As a result, crystals precipitated and the nematic phase wasnot maintained at a concentration of 3% or more.

Compatibility of Compound (1-2-3-25) at a Low Temperature

Compatibility, at a low temperature, namely, at −10° C. for 30 days, of3-(trans-4-(2,3-difluoro-4-ethyloxyphenyl)cyclohexyl)-6-propylcyclohexene (compound 1-2-3-25) obtained in Example8 was measured by using base liquid crystals (ii). As a result, thenematic phase was maintained at a concentration of 10% or less.

The findings show that compound (1-2-3-25) is superior to comparativecompound (Ex-3) in solubility in base liquid crystals at a lowtemperature, and useful as a liquid crystal compound.

In a manner similar to the synthetic methods described in Examples 1 to11, compounds as shown below can be prepared: compounds (1-1-1-1) to(1-1-1-24), (1-1-2-1) to (1-1-2-48), (1-2-1-1) to (1-2-1-24), (1-2-2-1)to (1-2-2-48), (1-2-3-1) to (1-2-3-48), (1-2-4-1) to (1-2-4-48),(1-3-1-1) to (1-3-1-24), (1-3-2-1) to (1-3-2-48), (1-3-3-1) to(1-3-3-48), (1-4-1-1) to (1-4-1-17), (1-4-2-1) to (1-4-2-34), (1-4-3-1)to (1-4-3-34), (1-4-4-1) to (1-4-4-34), (1-4-5-1) to (1-4-5-34),(1-4-6-1) to (1-4-6-34), (1-5-1-1) to (1-5-1-17), (1-5-2-1) to(1-5-2-34), (1-5-3-1) to (1-5-3-34), (1-5-4-1) to (1-5-4-34), (1-5-5-1)to (1-5-5-34), (1-5-6-1) to (1-5-6-34) and (1-5-7-1) to (1-5-7-34). Dataadded thereto are described as values obtained by measurement inaccordance with the techniques described above. As a transitiontemperature, an intrinsic value of the compound was described, and as amaximum temperature (T_(NI)), dielectric anisotropy (Δ∈) and opticalanisotropy (Δn), extrapolated values converted according to theextrapolation method from measured values of the sample prepared bymixing the compound with base liquid crystals (i) or (ii) weredescribed.

Examples of Liquid Crystal Compositions

Hereinafter, liquid crystal compositions obtained according to theinvention will be explained in detail by way of Examples. The liquidcrystal compounds used in Examples are described using symbols based ondefinitions in the Table below. In addition, a configuration of1,4-cyclohexylene in the Table is trans. Unless otherwise noted, eachratio (percentage) of compounds is expressed in terms of weight percent(% by weight) based on the total weight of a liquid crystal composition.Values of characteristics of the liquid crystal composition obtained areshown in the last part of each Example.

A method for description of compounds using symbols is shown below. Inaddition, the number as described in a part of the liquid crystalcompound used in each Example corresponds to the number of compound ofcomponents A to E described above. When a symbol “-” is simply describedwithout describing the number of compound, the symbol means that thecompound is any other compound that does not correspond to thecomponents.

Table Method for Description of Compounds using Symbols R—(A₁)—Z₁— . . .—Z_(n)—(A_(n))—R′ 1) Left-terminal Group R— Symbols C_(n)H_(2n+1)— n-C_(n)H_(2n+1)O— nO— C_(m)H_(2m+1)OC_(n)H_(2n)— mOn- CH₂═CH— V—C_(n)H_(2n+1)—CH═CH— nV— CH₂═CH—C_(n)H_(2n)— Vn-C_(m)H_(2m+1)—CH═CH—C_(n)H_(2n)— mVn- CF₂═CH— VFF— CF₂═CH—C_(n)H_(2n)—VFFn- 2) Right-terminal Group —R′ Symbols —C_(n)H_(2n+1) -n—OC_(n)H_(2n+1) —On —CH═CH₂ —V —CH═CH—C_(n)H_(2n+1) —Vn—C_(n)H_(2n)—CH═CH₂ -nV —C_(m)H_(2m)—CH═CH—C_(n)H_(2n+1) -mVn —CH═CF₂—VFF —COOCH₃ —EMe —F —F —Cl —CL —CN —C —OCF₃ —OCF3 3) Bonding Group—Z_(n)— Symbols —C_(n)H_(2n)— n —COO— E —CH═CH— V —CH₂O— 1O —OCH₂— O1—CF₂O— X —C≡C— T 4) Ring Structure —A_(n)— Symbols

B

B (F)

B (2F)

B (2F,3F)

B (F,F)

B (2F,5F)

Pr

Py

H

G

Gd

Cx

Ch 5) Examples of Description

Values of characteristics were determined according to methods asdescribed below. Most of the measuring methods are described in EIAJED-2521A of the Standard of Electronic Industries Association of Japan,or modified thereon.

(1) Maximum Temperature of a Nematic Phase (NI; ° C.)

A sample was placed on a hot plate of a melting point apparatus equippedwith a polarizing microscope, and heated at a rate of 1° C. per minute.Temperature when part of the sample changed from the nematic phase tothe isotropic liquid was measured. In the following, a maximumtemperature of the nematic phase may be occasionally abbreviated as“maximum temperature.”

(2) Minimum Temperature of a Nematic Phase (TC; ° C.)

Samples each having a nematic phase were kept in freezers at 0° C., −10°C., −20° C., −30° C. and −40° C. for 10 days, and then liquid crystalphases were observed. For example, when a sample maintained the nematicphase at −20° C. and changed to crystals or a smectic phase at −30° C.,TC was expressed as TC≦−20° C. In the following, a minimum temperatureof the nematic phase may be occasionally abbreviated as “minimumtemperature.”

(3) Optical Anisotropy (Δn; Measured at 25° C.)

Measurement was carried out by means of Abbe refractometer with apolarizing plate mounted on an ocular by using light at a wavelength of589 nanometers. A surface of a main prism was first rubbed in onedirection, and then a sample was added dropwise onto the main prism. Arefractive index (n∥) when the direction of polarized light was parallelto the direction of rubbing, and a refractive index (n⊥) when thedirection of polarized light was perpendicular to the direction ofrubbing were measured. A value of optical anisotropy (Δn) was calculatedfrom an equation: Δn=n∥−n⊥.

(4) Viscosity (Bulk Viscosity; η; Measured at 20° C.; mPa·s)

A cone-plate (E type) viscometer was used for measurement.

(5) Dielectric Anisotropy (Δ∈; Measured at 25° C.)

An ethanol (20 mL) solution of octadecyl triethoxysilane (0.16 mL) wasapplied to a well-washed glass substrate. After rotating the glasssubstrate with a spinner, the glass substrate was heated at 150° C. for1 hour. A VA device in which a distance (cell gap) was 20 micrometerswas assembled from two glass substrates.

In a similar manner, a polyamide alignment film was prepared on theglass substrate. After rubbing treatment was applied to the alignmentfilm obtained on the glass substrate, a TN device in which a distance(cell gap) between two glass substrates was 9 micrometers and a twistangle was 80 degrees was assembled.

A sample (a liquid crystal composition, or a mixture of a liquid crystalcompound and base liquid crystals) was put in the VA device obtained, avoltage of 0.5 V (1 kHz, sine waves) was applied to the device, and adielectric constant (∈∥) in the major axis direction of liquid crystalmolecules was measured.

Moreover, a sample (a liquid crystal composition, or a mixture of aliquid crystal compound and base liquid crystals) was put in the TNdevice obtained, a voltage of 0.5 V (1 kHz, sine waves) was applied tothe device, and a dielectric constant (∈⊥) in the minor axis directionof the liquid crystal molecules was measured.

A value of dielectric anisotropy was calculated from an equation:Δ∈=∈∥−∈⊥.

A composition in which the value is negative is a composition having anegative dielectric anisotropy

(6) Voltage Holding Ratio (VHR; Measured at 25° C. And 100° C.; %)

A sample was put in a cell having a polyimide alignment film in which adistance (cell gap) between two glass substrates was 6 micrometers, andthus a TN device was prepared. A pulse voltage (60 microseconds at 5 V)was applied to the device at 25° C., and thus the TN device was charged.A waveform of the voltage applied to the TN device was observed by meansof a cathode-ray oscilloscope, and an area between a voltage curve and ahorizontal axis in a unit cycle (16.7 milliseconds) was determined.After removing the TN device, an area was determined from the waveformof the applied voltage in a similar manner. A value of voltage holdingratio (%) was calculated from an equation: (voltage holdingratio)=(value of area with a TN device)/(value of area with no TNdevice)×100.

The thus obtained voltage holding ratio was described as “VHR-1.” Next,the TN device was heated at 100° C. for 250 hours. After the TN devicewas returned to 25° C., a voltage holding ratio was measured in asimilar manner as described above. A voltage holding ratio obtainedafter the heating test described above was conducted was described as“VHR-2.” In addition, the heating test is an accelerated test and wasused as a test corresponding to a test of durability of the TN devicefor a long period of time.

Use Example 1

3-HCx-5 (1-1-1-3) 6% 4-HHCx-5 (1-2-1-4) 3% 2-BEB(F)-C (5-14) 5%3-BEB(F)-C (5-14) 4% 4-BEB(F)-C (5-14) 6% 1V2-BEB(F,F)-C (5-15) 16%3-HB-O2 (12-5) 10% 3-HH-4 (12-1) 3% 3-HHB-F (3-1) 3% 3-HHB-1 (13-1) 8%3-HHB-O1 (13-1) 4% 3-HBEB-F (3-37) 4% 3-HHEB-F (3-10) 7% 5-HHEB-F (3-10)4% 3-H2BTB-2 (13-17) 4% 3-H2BTB-3 (13-17) 4% 3-H2BTB-4 (13-17) 4%3-HB(F)TB-2 (13-18) 5% NI = 87.3° C.; Δn = 0.134, Δε = 25.6; Vth = 1.06V.

Use Example 2

5-HHCx-3 (1-2-1-2) 3% 3-HCxO1H-5 (1-3-1-18) 3% 2-HB-C (5-1) 5% 3-HB-C(5-1) 12% 3-HB-O2 (12-5) 15% 2-BTB-1 (12-10) 3% 3-HHB-F (3-1) 4% 3-HHB-1(13-1) 4% 3-HHB-O1 (13-1) 5% 3-HHB-3 (13-1) 14% 3-HHEB-F (3-10) 4%5-HHEB-F (3-10) 4% 2-HHB(F)-F (3-2) 5% 3-HHB(F)-F (3-2) 7% 5-HHB(F)-F(3-2) 7% 3-HHB(F,F)-F (3-3) 5% NI = 102.5° C.; Δn = 0.099; Δε = 4.3; Vth= 2.66 V; η = 18.7 mPa · s.

Use Example 3

2-HHCx-3 (1-2-1-5) 3% 3-HCxVH-5 (1-3-1-13) 3% 3-BEB(F)-C (5-14) 8%3-HB-C (5-1) 8% V-HB-C (5-1) 8% 1V-HB-C (5-1) 8% 3-HB-O2 (12-5) 3%3-HH-2V (12-1) 14% 3-HH-2V1 (12-1) 7% V2-HHB-1 (13-1) 12% 3-HHB-1 (13-1)5% 3-HHEB-F (3-10) 4% 3-H2BTB-2 (13-17) 6% 3-H2BTB-3 (13-17) 6%3-H2BTB-4 (13-17) 5% NI = 98.0° C.; Δn = 0.130; Δε = 8.1; Vth = 2.23 V;η = 15.6 mPa · s.

A pitch when 0.25 part of optically active compound (Op-5) was added to100 parts of the composition was 60.2 micrometers.

Use Example 4

2-HHCx-5 (1-2-1-6) 3% 3-HHCx-5 (1-2-1-1) 3% 5-BEB(F)-C (5-14) 4% V-HB-C(5-1) 11% 5-PyB-C (5-9) 6% 4-BB-3 (12-8) 11% 3-HH-2V (12-1) 10% 5-HH-V(12-1) 11% V-HHB-1 (13-1) 7% V2-HHB-1 (13-1) 15% 3-HHB-1 (13-1) 4%1V2-HBB-2 (13-4) 10% 3-HHEBH-3 (14-6) 5% NI = 92.6° C.; Δn = 0.114; Δε =4.3; Vth = 2.51 V; η = 15.5 mPa · s.

Use Example 5

1-BHCx-3 (1-2-3-4) 4% 3-CxHVH-5 (1-2-1-20) 4% 1V2-BEB(F,F)-C (5-15) 3%3-HB-C (5-1) 18% 2-BTB-1 (12-10) 10% 5-HH-VFF (—) 30% 3-HHB-1 (13-1) 4%VFF-HHB-1 (—) 3% VFF2-HHB-1 (—) 11% 3-H2BTB-2 (13-17) 5% 3-H2BTB-3(13-17) 4% 3-H2BTB-4 (13-17) 4% NI = 90.2° C.; Δn = 0.129; Δε = 4.2; Vth= 2.79 V; η = 11.8 mPa · s.

Use Example 6

3-HCx-5 (1-1-1-3) 5% 3-HHCx-2V (1-2-1-9) 3% 5-HB-CL (2-1) 16% 3-HH-4(12-1) 12% 3-HH-5 (12-1) 4% 3-HHB-F (3-1) 4% 3-HHB-CL (3-1) 3% 4-HHB-CL(3-1) 4% 3-HHB(F)-F (3-2) 10% 4-HHB(F)-F (3-2) 9% 5-HHB(F)-F (3-2) 5%7-HHB(F)-F (3-2) 4% 5-HBB(F)-F (3-23) 4% 1O1-HBBH-5 (14-1) 3%3-HHBB(F,F)-F (4-6) 2% 4-HHBB(F,F)-F (4-6) 3% 5-HHBB(F,F)-F (4-6) 3%3-HH2BB(F,F)-F (4-15) 3% 4-HH2BB(F,F)-F (4-15) 3% NI = 111.9° C.; Δn =0.089; Δε = 3.2; Vth = 2.69 V; η = 7.6 mPa · s.

Use Example 7

2-HHCx-3 (1-2-1-5) 3% 5-HHCx-3 (1-2-1-2) 3% 3-HHB(F,F)-F (3-3) 9%3-H2HB(F,F)-F (3-15) 8% 4-H2HB(F,F)-F (3-15) 8% 5-H2HB(F,F)-F (3-15) 8%3-HBB(F,F)-F (3-24) 21% 5-HBB(F,F)-F (3-24) 20% 3-H2BB(F,F)-F (3-27) 7%5-HHBB(F,F)-F (4-6) 3% 5-HHEBB-F (4-17) 2% 3-HH2BB(F,F)-F (4-15) 3%1O1-HBBH-4 (14-1) 2% 1O1-HBBH-5 (14-1) 3% NI = 98.0° C.; Δn = 0.111, Δε= 8.6; Vth = 1.80 V.

Use Example 8

4-HHCx-5 (1-2-1-4) 4% 3-HCxO1H-5 (1-3-1-18) 4% 5-HB-F (2-1) 10% 6-HB-F(2-1) 9% 7-HB-F (2-1) 7% 2-HHB-OCF3 (3-1) 7% 3-HHB-OCF3 (3-1) 7%4-HHB-OCF3 (3-1) 7% 5-HHB-OCF3 (3-1) 5% 3-HH2B-OCF3 (3-4) 4% 5-HH2B-OCF3(3-4) 4% 3-HHB(F,F)-OCF2H (3-3) 4% 3-HHB(F,F)-OCF3 (3-3) 5% 3-HH2B(F)-F(3-5) 3% 3-HBB(F)-F (3-23) 5% 5-HBB(F)-F (3-23) 10% 5-HBBH-3 (14-1) 2%3-HB(F)BH-3 (14-2) 3% NI = 91.8° C.; Δn = 0.090; Δε = 3.9; Vth = 2.70 V;η = 15.4 mPa · s.

Use Example 9

2-HHCx-5 (1-2-1-6) 3% 3-HHCx-5 (1-2-1-1) 3% 5-HB-CL (2-2) 11% 3-HH-4(12-1) 8% 3-HHB-1 (13-1) 3% 3-HHB(F,F)-F (3-3) 8% 3-HBB(F,F)-F (3-24)20% 5-HBB(F,F)-F (3-24) 15% 3-HHEB(F,F)-F (3-12) 10% 4-HHEB(F,F)-F(3-12) 3% 5-HHEB(F,F)-F (3-12) 3% 2-HBEB(F,F)-F (3-39) 3% 3-HBEB(F,F)-F(3-39) 4% 5-HBEB(F,F)-F (3-39) 3% 3-HHBB(F,F)-F (4-6) 3% NI = 79.9° C.;Δn = 0.099; Δε = 8.0; Vth = 1.57 V; η = 21.2 mPa · s.

Use Example 10

3-HCxVH-5 (1-3-1-13) 3% 1-BHCx-3 (1-2-3-4) 3% 3-HB-CL (2-2) 2% 5-HB-CL(2-2) 4% 3-HHB-OCF3 (3-2) 5% 3-H2HB-OCF3 (3-13) 5% 5-H4HB-OCF3 (3-19)15% V-HHB(F)-F (3-2) 5% 3-HHB(F)-F (3-2) 5% 5-HHB(F)-F (3-2) 5%3-H4HB(F,F)-CF3 (3-21) 8% 5-H4HB(F,F)-CF3 (3-21) 10% 5-H2HB(F,F)-F(3-15) 5% 5-H4HB(F,F)-F (3-21) 7% 2-H2BB(F)-F (3-26) 5% 3-H2BB(F)-F(3-26) 8% 3-HBEB(F,F)-F (3-39) 5% NI = 80.2° C.; Δn = 0.098; Δε = 8.0;Vth = 2.00 V; η = 26.9 mPa · s.

Use Example 11

4-HHCx-5 (1-2-1-4) 2% 3-CxHVH-5 (1-2-1-20) 4% 5-HB-CL (2-2) 17%7-HB(F,F)-F (2-4) 3% 3-HH-4 (12-1) 10% 3-HH-5 (12-1) 5% 3-HB-O2 (12-5)15% 3-HHB-1 (13-1) 8% 3-HHB-O1 (13-1) 5% 2-HHB(F)-F (3-2) 7% 3-HHB(F)-F(3-2) 7% 5-HHB(F)-F (3-2) 7% 3-HHB(F,F)-F (3-3) 6% 3-H2HB(F,F)-F (3-15)2% 4-H2HB(F,F)-F (3-15) 2% NI = 79.3° C.; Δn = 0.076; Δε = 2.3; Vth =2.39 V; η = 14.0 mPa · s.

Use Example 12

3-CxHVH-5 (1-2-1-20) 3% 3-HHCx-2V (1-2-1-9) 3% 5-HB-CL (2-2) 3%7-HB(F)-F (2-3) 7% 3-HH-4 (12-1) 9% 3-HH-EMe (12-2) 20% 3-HHEB-F (3-10)8% 5-HHEB-F (3-10) 8% 3-HHEB(F,F)-F (3-12) 10% 4-HHEB(F,F)-F (3-12) 5%4-HGB(F,F)-F (3-103) 5% 5-HGB(F,F)-F (3-103) 6% 2-H2GB(F,F)-F (3-106) 4%3-H2GB(F,F)-F (3-106) 5% 5-GHB(F,F)-F (3-109) 4% NI = 88.1° C.; Δn =0.066; Δε = 4.8; Vth = 1.80 V; η = 19.1 mPa · s.

Use Example 13

5-HHCx-3 (1-2-1-2) 3% 3-HCxO1H-5 (1-3-1-18) 3% 3-HB-O2 (12-5) 10%5-HB-CL (2-2) 13% 3-HBB(F,F)-F (3-24) 7% 3-PyB(F)-F (2-15) 10%5-PyB(F)-F (2-15) 10% 3-PyBB-F (3-80) 10% 4-PyBB-F (3-80) 10% 5-PyBB-F(3-80) 10% 5-HBB(F)B-2 (14-5) 7% 5-HBB(F)B-3 (14-5) 7% NI = 95.2° C.; Δn= 0.180; Δε = 7.7; Vth = 1.93 V.

Use Example 14

3-HCx-5 (1-1-1-3) 4% 5-HHCx-3 (1-2-1-2) 3% 3-HH-O1 (12-1) 8% 5-HH-O1(12-1) 4% 3-HH-4 (12-1) 5% 3-HB(2F,3F)-O2 (6-1) 12% 5-HB(2F,3F)-O2 (6-1)21% 2-HHB(2F,3F)-1 (7-1) 5% 3-HHB(2F,3F)-1 (7-1) 7% 3-HHB(2F,3F)-O2(7-1) 11% 5-HHB(2F,3F)-O2 (7-1) 20% NI = 62.4° C.; Δn = 0.074; η = 21.6mPa · s; Δε = −3.9.

Use Example 15

3-HHCx-5 (1-2-1-1) 5% 4-HHCx-5 (1-2-1-4) 3% 3-HB-O1 (12-5) 15% 3-HH-4(12-1) 5% 3-HB(2F,3F)-O2 (6-1) 12% 5-HB(2F,3F)-O2 (6-1) 12%2-HHB(2F,3F)-1 (7-1) 12% 3-HHB(2F,3F)-1 (7-1) 12% 3-HHB(2F,3F)-O2 (7-1)8% 5-HHB(2F,3F)-O2 (7-1) 10% 3-HHB-O1 (13-1) 6% NI = 86.9° C.; Δn =0.087; Δε = −3.0.

Use Example 16

3-CxHB(2F,3F)-O2 (1-2-3-25) 4% 5-CxHB(2F,3F)-O2 (1-2-3-26) 4% 3-HB-O1(12-5) 15% 3-HH-4 (12-1) 5% 3-HB(2F,3F)-O2 (6-1) 12% 5-HB(2F,3F)-O2(6-1) 12% 2-HHB(2F,3F)-1 (7-1) 12% 3-HHB(2F,3F)-1 (7-1) 10%3-HHB(2F,3F)-O2 (7-1) 7% 5-HHB(2F,3F)-O2 (7-1) 13% 3-HHB-1 (13-1) 6% NI= 83.6° C.; Δn = 0.090; η = 36.1 mPa · s; Δε = −3.5.

Use Example 17

3-CxHB(2F,3F)-O2 (1-2-3-25) 3% 5-CxHB(2F,3F)-O2 (1-2-3-26) 3% 3-HH-4(12-1) 8% 3-H2B(2F,3F)-O2 (6-4) 22% 5-H2B(2F,3F)-O2 (6-4) 22%3-HHB(2F,3CL)-O2 (7-12) 3% 5-HHB(2F,3CL)-O2 (7-12) 2% 3-HBB(2F,3F)-O2(7-7) 7% 5-HBB(2F,3F)-O2 (7-7) 9% V-HHB-1 (13-1) 6% 3-HHB-3 (13-1) 6%3-HHEBH-3 (14-6) 3% 3-HHEBH-4 (14-6) 3% 3-HHEBH-5 (14-6) 3% NI = 89.9°C.; Δn = 0.099; η = 28.3 mPa · s; Δε = −4.1.

A pitch when 0.25 part of optically active compound (Op-05) was added to100 parts of the composition was 60.3 micrometers.

Use Example 18

3-HCx1OB(2F,3F)-O2 (1-3-2-40) 3% 5-HCx1OB(2F,3F)-O2 (1-3-2-39) 3%3-HB-O1 (12-5) 15% 3-HH-4 (12-1) 5% 3-HB(2F,3F)-O2 (6-1) 12%5-HB(2F,3F)-O2 (6-1) 12% 2-HHB(2F,3F)-1 (7-1) 10% 3-HHB(2F,3F)-1 (7-1)12% 3-HHB(2F,3F)-O2 (7-1) 9% 5-HHB(2F,3F)-O2 (7-1) 13% 6-HEB(2F,3F)-O2(7-1) 6%

Use Example 19

3-HCxB(2F,3F)-O2 (1-3-2-25) 3% 5-HCxB(2F,3F)-O2 (1-3-2-26) 3% 2-HH-5(12-1) 3% 3-HH-4 (12-1) 15% 3-HH-5 (12-1) 4% 3-HB-O2 (12-5) 12%3-H2B(2F,3F)-O2 (6-4) 15% 5-H2B(2F,3F)-O2 (6-4) 15% 3-HHB(2F,3CL)-O2(7-12) 3% 2-HBB(2F,3F)-O2 (7-7) 3% 3-HBB(2F,3F)-O2 (7-7) 5%5-HBB(2F,3F)-O2 (7-7) 9% 3-HHB-1 (13-1) 3% 3-HHB-3 (13-1) 4% 3-HHB-O1(13-1) 3%

Use Example 20

3-CxH1OB(2F,3F)-O2 (1-2-3-41) 3% 5-CxH1OB(2F,3F)-O2 (1-2-3-42) 3%3-HB-O1 (12-5) 15% 3-HH-4 (12-1) 5% 3-HB(2F,3F)-O2 (6-1) 12%5-HB(2F,3F)-O2 (6-1) 12% 2-HHB(2F,3F)-1 (7-1) 12% 3-HHB(2F,3F)-1 (7-1)10% 3-HHB(2F,3F)-O2 (7-1) 9% 5-HHB(2F,3F)-O2 (7-1) 13% 3-HHB-1 (13-1) 6%

Use Example 21

3-CxB(2F,3F)-O2 (1-1-2-25) 3% 5-CxB(2F,3F)-O2 (1-2-2-26) 3% 2-BEB(F)-C(5-14) 3% 3-BEB(F)-C (5-14) 4% 4-BEB(F)-C (5-14) 8% 1V2-BEB(F,F)-C(5-15) 16% 3-HB-O2 (12-5) 10% 3-HH-4 (12-1) 3% 3-HHB-F (3-1) 3% 3-HHB-1(13-1) 8% 3-HHB-O1 (13-1) 4% 3-HBEB-F (3-37) 4% 3-HHEB-F (3-10) 7%5-HHEB-F (3-10) 7% 3-H2BTB-2 (13-17) 4% 3-H2BTB-3 (13-17) 4% 3-H2BTB-4(13-17) 4% 3-HB(F)TB-2 (13-18) 5%

Use Example 22

3-HCx1OB(2CF3,3F)-O2 (1-3-2-44) 3% 5-HCx1OB(2CF2H,3F)-O2 (1-3-2-46) 3%1V2-BEB(F,F)-C (5-15) 5% 3-HB-C (5-1) 18% 2-BTB-1 (12-10) 10% 5-HH-VFF(12-1) 30% 3-HHB-1 (13-1) 4% VFF-HHB-1 (13-1) 8% VFF2-HHB-1 (13-1) 6%3-H2BTB-2 (13-17) 5% 3-H2BTB-3 (13-17) 4% 3-H2BTB-4 (13-17) 4%

Use Example 23

3-CxHB(2F,3F)-O2 (1-2-3-25) 3% 5-CxHB(2F,3F)-O2 (1-2-3-26) 3% 2-HB-C(5-1) 5% 3-HB-C (5-1) 12% 3-HB-O2 (12-5) 15% 2-BTB-1 (12-10) 3% 3-HHB-F(3-1) 4% 3-HHB-1 (13-1) 8% 3-HHB-O1 (13-1) 5% 3-HHB-3 (13-1) 14%3-HHEB-F (3-10) 4% 5-HHEB-F (3-10) 4% 2-HHB(F)-F (3-2) 4% 3-HHB(F)-F(3-2) 4% 5-HHB(F)-F (3-2) 7% 3-HHB(F,F)-F (3-3) 5%

Use Example 24

3-CxHB(2F,3F)-O2 (1-2-3-25) 3% 3-HCx1OB(2F,3F)-O2 (1-3-2-40) 3% 5-HB-CL(2-2) 16% 3-HH-4 (12-1) 12% 3-HH-5 (12-1) 4% 3-HHB-F (3-1) 4% 3-HHB-CL(3-1) 3% 4-HHB-CL (3-1) 4% 3-HHB(F)-F (3-2) 5% 4-HHB(F)-F (3-2) 9%5-HHB(F)-F (3-2) 9% 7-HHB(F)-F (3-2) 8% 5-HBB(F)-F (3-23) 3% 1O1-HBBH-5(14-1) 3% 3-HHBB(F,F)-F (4-6) 2% 4-HHBB(F,F)-F (4-6) 3% 5-HHBB(F,F)-F(4-6) 3% 3-HH2BB(F,F)-F (4-15) 3% 4-HH2BB(F,F)-F (4-15) 3%

Use Example 25

5-HCx1OB(2F,3F)-O2 (1-3-2-39) 3% 3-HCxB(2F,3F)-O2 (1-3-2-25) 3% 5-HB-CL(2-2) 3% 7-HB(F)-F (2-3) 7% 3-HH-4 (12-1) 9% 3-HH-EMe (12-2) 23%3-HHEB-F (3-10) 8% 5-HHEB-F (3-10) 8% 3-HHEB(F,F)-F (3-12) 6%4-HHEB(F,F)-F (3-12) 3% 4-HGB(F,F)-F (3-103) 5% 5-HGB(F,F)-F (3-103) 6%2-H2GB(F,F)-F (3-106) 4% 3-H2GB(F,F)-F (3-106) 5% 5-GHB(F,F)-F (3-109)7%

INDUSTRIAL APPLICABILITY

A compound of the invention has both a high clearing point and a lowcrystallization temperature, and thus has a wide temperature range of aliquid crystal phase, and also an excellent solubility in other liquidcrystal compounds. The compound of the invention further has generalphysical properties necessary for the compound, namely, stability toheat, light and so forth, a suitable optical anisotropy and a suitabledielectric anisotropy furthermore. A liquid crystal composition of theinvention contains at least one of the compounds, and has a high maximumtemperature of a nematic phase, a low minimum temperature of the nematicphase, a small viscosity, a suitable optical anisotropy and a lowthreshold voltage. A liquid crystal display device of the inventionincludes the composition and has a wide temperature range in which thedevice can be used, a short response time, a large contrast ratio and alow driving voltage, and therefore can be used for a liquid crystalprojector, a liquid crystal television and so forth.

1. A compound represented by formula (1):

wherein, in formula (1), Ra and Rb are independently hydrogen, halogenor alkyl having 1 to 10 carbons, and in the alkyl, arbitrary —CH₂— maybe replaced by —O—, —S—, —CO— or —SiH₂—, and arbitrary —(CH₂)₂— may bereplaced by —CH═CH— or —C≡C—; A¹, A², A³ and A⁴ are independently1,4-cyclohexylene, 1,4-phenylene, cyclohexene-1,4-diyl,cyclohexene-3,6-diyl, decahydronaphthalene-2,6-diyl,1,2,3,4-tetrahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl, and inthe rings, one of —CH₂— may be replaced by —O—, —S—, —CO— or —SiH₂—, andarbitrary —(CH₂)₂— may be replaced by —CH═CH—, and in the rings,arbitrary hydrogen may be replaced by halogen, —CF₃, —CHF₂, —CH₂F,—OCF₃, —OCHF₂ or —OCH₂F; Z¹, Z², Z³ and Z⁴ are independently a singlebond or alkylene having 1 to 4 carbons, and in the alkylene, arbitrary—CH₂— may be replaced by —O—, —S— or —SiH₂—, and arbitrary —(CH₂)₂— maybe replaced by —CH═CH— or —C≡C—; m, n, q and r are independently 0, 1 or2, and a sum of m, n, q and r is 1, 2, 3 or 4; and when a sum of m, n, qand r is 1, Ra and Rb are independently hydrogen, halogen or alkylhaving 1 to 10 carbons, and in the alkyl, arbitrary —CH₂— may bereplaced by —O—, —S—, —CO— or —SiH₂—, and arbitrary —(CH₂)₂—may bereplaced by —CH═CH— or —C≡C—; A¹, A², A³ and A⁴ are independently1,4-cyclohexylene, 1,4-phenylene in which one or more of hydrogen isreplaced by halogen, cyclohexene-1,4-diyl, cyclohexene-3,6-diyl,decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,6-diyl ornaphthalene-2,6-diyl, and in the rings, one of —CH₂— may be replaced by—O—, —S—, —CO—, or —SiH₂—, and arbitrary —(CH₂)₂— may be replaced by—CH═CH—, and in the rings, arbitrary hydrogen may be replaced byhalogen, —CF₃, —CHF₂, —CH₂F, —OCF₃, —OCHF₂ or —OCH₂F; and Z¹, Z², Z³ andZ⁴ are independently a single bond or alkylene having 1 to 4 carbons,and in the alkylene, arbitrary —CH₂— may be replaced by —O—, —S— or—SiH₂—, and arbitrary —(CH₂)₂— may be replaced by —CH═CH— or —C≡C—. 2.The compound according to claim 1, represented by formula (1-1) toformula (1-8):

wherein, in formula (1-1) to formula (1-8), Ra and Rb are independentlyhydrogen, halogen or alkyl having 1 to 10 carbons, and in the alkyl,arbitrary —CH₂— may be replaced by —O—, —S—, —CO— or —SiH₂—, andarbitrary —(CH₂)₂— may be replaced by —CH═CH— or —C≡C—; A¹¹, A²¹, A³²,A⁴¹, A⁴² and A⁴³ are independently 1,4-cyclohexylene,cyclohexenylene-1,4-diyl, 1,4-phenylene, cyclohexene-2,5-diyl,decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,5-diyl ornaphthalene-2,6-diyl, A³¹ is 1,4-cyclohexylene, cyclohexene-1,4-diyl,1,4-phenylene in which one or more of hydrogen is replaced by halogen,cyclohexene-3,6-diyl, decahydronaphthalene-2,6-diyl,1,2,3,4-tetrahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl, and inthe rings, one of —CH₂— may be replaced by —O—, —S—, —CO—, or —SiH₂—,and arbitrary —(CH₂)₂— may be replaced by —CH═CH—, and in the rings, oneof hydrogen may be replaced by halogen, —CF₃, —CHF₂, —CH₂F, —OCF₃,—OCHF₂ or —OCH₂F; and Z¹¹, Z²¹, Z³¹, Z³², Z⁴¹, Z⁴² and Z⁴³ areindependently a single bond or alkylene having 1 to 4 carbons, and inthe alkylene, arbitrary —CH₂— may be replaced by —O—, —S— or —SiH₂—, andarbitrary —(CH₂)₂— may be replaced by —CH═CH— or —C≡C—.
 3. The compoundaccording to claim 2, wherein, in formula (1-1) to formula (1-8), Ra andRb are independently fluorine, alkyl having 1 to 10 carbons, alkenylhaving 2 to 10 carbons, alkoxy having 1 to 9 carbons, alkoxyalkyl having2 to 9 carbons, alkenyloxy having 3 to 9 carbons, polyfluoroalkyl having2 to 10 carbons, polyfluoroalkoxy having 1 to 9 carbons orpolyfluoroalkenyl having 2 to 10 carbons; A¹¹, A²¹, A³², A⁴¹, A⁴² andA⁴³ are independently 1,4-cyclohexylene, 1,4-phenylene,cyclohexene-1,4-diyl, cyclohexene-3,6-diyl, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene, decahydronaphthalene-2,6-diyl,1,2,3,4-tetrahydronaphthalene-2,6-diyl or naphthalene-2,6-diyl, and A³¹is 1,4-cyclohexylene, cyclohexene-1,4-diyl, cyclohexene-3,6-diyl,2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene,decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,6-diyl ornaphthalene-2,6-diyl; and Z¹¹, Z²¹, Z³¹, Z³², Z⁴¹, Z⁴² and Z⁴³ areindependently a single bond, —(CH₂)₂—, —CH—CH—, —CH₂O—, —OCH₂—,—(CH₂)₄—, —C≡C—, —CH₂SiH₂—, —SiH₂CH₂—, —O(CH₂)₂O—, —CH═CH—CH₂O— or—OCH₂—CH═CH—.
 4. The compound according to claim 2, wherein, in formula(1-1) to formula (1-5), Ra and Rb are independently fluorine, alkylhaving 1 to 8 carbons, alkenyl having 2 to 8 carbons, alkoxy having 1 to7 carbons, alkoxyalkyl having 2 to 7 carbons or alkenyloxy having 3 to 7carbons; A²¹, A³², A⁴¹ and A⁴² are independently 1,4-cyclohexylene,1,4-phenylene, cyclohexene-1,4-diyl, cyclohexene-3,6-diyl,2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene, and A³¹ is1,4-cyclohexylene, cyclohexene-1,4-diyl, cyclohexene-3,6-diyl,2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene; and Z²¹, Z³¹, Z³², Z⁴¹and Z⁴² are independently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O—,—OCH₂—, —(CH₂)₄— or —C═C—.
 5. The compound according to claim 2,wherein, in formula (1-1) to formula (1-3), Ra and Rb are independentlyalkyl having 1 to 5 carbons, alkenyl having 2 to 5 carbons or alkoxyhaving 1 to 4 carbons; A²¹, A³¹, A³² and A⁴² are independently1,4-cyclohexylene; and Z²¹, Z³¹, Z³² and Z⁴² are independently a singlebond, —(CH₂)₂— or —CH═CH—.
 6. The compound according to claim 2,wherein, in formula (1-1) to formula (1-3), A²¹, A³¹, A³² and A⁴² areindependently 1,4-cyclohexylene, and Z²¹, Z³¹, Z³² and Z⁴² are a singlebond. 7-10. (canceled)
 11. The compound according to claim 2,represented by any one of formula (1-1-1) to formula (1-1-2), formula(1-2-1) to formula (1-2-4), formula (1-3-1) to formula (1-3-3), formula(1-4-1) to formula (1-4-6) and formula (1-5-1) to formula (1-5-7):

wherein, in formula (1-1-1), formula (1-2-1) to formula (1-2-4), formula(1-3-1) to formula (1-3-3), formula (1-4-1) to formula (1-4-6) andformula (1-5-1) to formula (1-5-7), Ra and Rb are independently alkylhaving 2 to 10 carbons, alkoxy having 1 to 9 carbons or alkenyl having 2to 10 carbons; Z²¹, Z³¹, Z³², Z⁴¹ and Z⁴² are independently a singlebond, —(CH₂)₂—, —CH═CH—, —CH₂O—, —OCH₂—, —CF₂O— or —OCF₂—; X¹² to X¹⁴,X²² to X²⁴, X³² to X³⁴, and X⁴² to X⁴⁴ are independently fluorine orhydrogen; in formula (1-1-2), R³ and R⁴ are independently alkyl having 1to 10 carbons, alkenyl having 2 to 10 carbons, alkoxy having 1 to 9carbons, alkoxyalkyl having 2 to 9 carbons or alkenyloxy having 2 to 9carbons; X¹⁰, X¹⁰, X³⁰ and X⁴⁰ are independently hydrogen or fluorine,at least one of X¹⁰, X²⁰, X³⁰ and X⁴⁰ is fluorine; and Z³¹ is a singlebond, —(CH₂)₂—, —CH═CH—, —CH₂O—, —OCH₂—, —CF₂O— Or —OCF₂—.
 12. Thecompound according to claim 2, represented by any one of formulas(1-1-1), (1-2-1) and (1-3-1):

wherein, in formulas (1-1-1), (1-2-1) and (1-3-1), Ra and Rb areindependently alkyl having 1 to 8 carbons, alkoxy having 1 to 7 carbonsor alkenyl having 2 to 8 carbons; and Z²¹, Z³¹, Z³² and Z⁴¹ areindependently a single bond, —(CH₂)₂—, —CH═CH—, —CH₂O— or —OCH₂—. 13.The compound according to claim 12, wherein, in formulas (1-1-1),(1-2-1) and (1-3-1), Ra and Rb are alkyl having 1 to 5 carbons oralkenyl having 2 to 5 carbons; and Z²¹, Z³¹, Z³² and Z⁴¹ areindependently a single bond or —CH═CH—.
 14. The compound according toclaim 12, wherein, in formulas (1-1-1), (1-2-1) and (1-3-1), one of Raand Rb is alkenyl having 2 to 5 carbons; and Z²¹, Z³¹, Z³² and Z⁴¹ areindependently a single bond or —CH═CH—.
 15. The compound according toclaim 12, wherein, in formulas (1-1-1), (1-2-1) and (1-3-1), Ra and Rbare alkenyl having 2 to 5 carbons, and Z²¹, Z³¹, Z³² and Z⁴¹ areindependently a single bond or —CH═CH—. 16-20. (canceled)
 21. A liquidcrystal composition containing at least one compound according toclaim
 1. 22. The liquid crystal composition according to claim 21,further containing at least one compound selected from the group ofcompounds represented by formulas (2), (3) and (4):

wherein, in formulas (2) to (4), R⁹ is independently alkyl having 1 to10 carbons or alkenyl having 2 to 10 carbons, and in the alkyl and thealkenyl, arbitrary hydrogen may be replaced by fluorine and arbitrary—CH₂— may be replaced by —O—; X¹ is fluorine, chlorine, —OCF₃, —OCHF₂,—CF₃, —CHF₂, —CH₂F, —OCF₂CHF₂ or —OCF₂CHFCF₃; ring B¹, ring B² and ringB³ are independently 1,4-cyclohexylene, 1,3-dioxane-2,5-diyl,pyrimidine-2,5-diyl, 1-tetrahydropyran-2,5-diyl, 1,4-phenylene,2-fluoro-1,4-phenylene, 3-fluoro-1,4-phenylene or3,5-difluoro-1,4-phenylene; Z⁷ and Z⁸ are independently —(CH₂)₂—,—(CH₂)₄—, —COO—, —CF₂O—, —OCF₂—, —CH═CH—, —C≡C—, —CH₂O— or a singlebond; and L⁹ and L¹⁰ are independently hydrogen or fluorine.
 23. Theliquid crystal composition according to claim 21, further containing atleast one compound selected from the group of compounds represented byformula (5):

wherein, in formula (5), R¹⁰ is alkyl having 1 to 10 carbons or alkenylhaving 2 to 10 carbons, and in the alkyl and the alkenyl, arbitraryhydrogen may be replaced by fluorine and arbitrary —CH₂— may be replacedby —O—; X² is —C≡N or —C≡C—C≡N; ring C¹, ring C² and ring C³ areindependently 1,4-cyclohexylene, 1,4-phenylene in which arbitraryhydrogen may be replaced by fluorine, 1,3-dioxane-2,5-diyl,1-tetrahydropyran-2,5-diyl or pyrimidine-2,5-diyl; Z⁹ is —(CH₂)₂—,—COO—, —CF₂O—, —OCF₂—, —C≡C—, —CH₂O— or a single bond; L¹¹ and L¹² areindependently hydrogen or fluorine; and o is 0, 1 or 2, p is 0 or 1, anda sum of o and p is 0, 1, 2 or
 3. 24. The liquid crystal compositionaccording to claim 21, further containing at least one compound selectedfrom the group of compounds represented by formulas (6), (7), (8), (9),(10) and (11):

wherein, in formulas (6) to (11), R¹¹ and R¹² are independently alkylhaving 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in thealkyl and the alkenyl, arbitrary hydrogen may be replaced by fluorineand arbitrary —CH₂— may be replaced by —O—; ring D¹, ring D², ring D³and ring D⁴ are independently 1,4-cyclohexylene, 1,4-cyclohexenylene,1,4-phenylene in which arbitrary hydrogen may be replaced by fluorine,6-tetrahydropyran-2,5-diyl or decahydro-2,6-naphthalene; Z¹⁰, Z¹¹, Z¹²and Z¹³ are independently —(CH₂)₂—, —COO—, —CH₂O—, —OCF₂—, —OCF₂(CH₂)₂—or a single bond; L¹³ and L¹⁴ independently ndependently fluorine orchlorine; and q, r, s, t, u and v are independently 0 or 1, and a sum ofr, s, t and u is 1 or
 2. 25. The liquid crystal composition according toclaim 21, further containing at least one compound selected from thegroup of compounds represented by formulas (12), (13) and (14):

wherein, in formulas (12) to (14), R¹³ and R¹⁴ are independently alkylhaving 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in thealkyl and the alkenyl, arbitrary —CH₂— may be replaced by —O—; ring E¹,ring E² and ring E³ are independently 1,4-cyclohexylene,pyrimidine-2,5-diyl, 1,4-phenylene, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; and Z¹⁴ and Z¹⁵are independently —C≡C—, —COO—, —(CH₂)₂—, —CH═CH— or a single bond. 26.The liquid crystal composition according to claim 22, further containingat least one compound selected from the group of compounds representedby formula (5):

wherein, in formula (5), R¹⁰ is alkyl having 1 to 10 carbons or alkenylhaving 2 to 10 carbons, and in the alkyl and the alkenyl, arbitraryhydrogen may be replaced by fluorine and arbitrary —CH₂— may be replacedby —O—; X² is —C≡N or —C≡C—C≡N; ring C¹, ring C² and ring C³ areindependently 1,4-cyclohexylene, 1,4-phenylene in which arbitraryhydrogen may be replaced by fluorine, 1,3-dioxane-2,5-diyl,1-tetrahydropyran-2,5-diyl or pyrimidine-2,5-diyl; Z⁹ is —(CH₂)₂—,—COO—, —CF₂O—, —OCF₂—, —C≡C—, —CH₂O— or a single bond; L¹¹ and L¹² areindependently hydrogen or fluorine; and o is 0, 1 or 2, p is 0 or 1, anda sum of o and p is 0, 1, 2 or
 3. 27. The liquid crystal compositionaccording to claim 22, further containing at least one compound selectedfrom the group of compounds represented by formulas (12), (13) and (14):

wherein, in formulas (12) to (14), R¹³ and R¹⁴ are independently alkylhaving 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in thealkyl and the alkenyl, arbitrary —CH₂— may be replaced by —O—; ring E¹,ring E² and ring E³ are independently 1,4-cyclohexylene,pyrimidine-2,5-diyl, 1,4-phenylene, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; and Z¹⁴ and Z¹⁵are independently —C≡C—, —COO—, —(CH₂)₂—, —CH═CH— or a single bond. 28.The liquid crystal composition according to claim 23, further containingat least one compound selected from the group of compounds representedby formulas (12), (13) and (14):

wherein, in formulas (12) to (14), R¹³ and R¹⁴ are independently alkylhaving 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in thealkyl and the alkenyl, arbitrary —CH₂— may be replaced by —O—; ring E¹,ring E² and ring E³ are independently 1,4-cyclohexylene,pyrimidine-2,5-diyl, 1,4-phenylene, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; and Z¹⁴ and Z¹⁵are independently —C≡C—, —COO—, —(CH₂)₂—, —CH═CH— or a single bond. 29.The liquid crystal composition according to claim 24, further containingat least one compound selected from the group of compounds representedby formulas (12), (13) and (14):

wherein, in formulas (12) to (14), R¹³ and R¹⁴ are independently alkylhaving 1 to 10 carbons or alkenyl having 2 to 10 carbons, and in thealkyl and the alkenyl, arbitrary —CH₂— may be replaced by —O—; ring E¹,ring E² and ring E³ are independently 1,4-cyclohexylene,pyrimidine-2,5-diyl, 1,4-phenylene, 2-fluoro-1,4-phenylene,3-fluoro-1,4-phenylene or 2,5-difluoro-1,4-phenylene; and Z¹⁴ and Z¹⁵are independently —C≡C—, —COO—, —(CH₂)₂—, —CH═CH— or a single bond. 30.The liquid crystal composition according to claim 21, further containingat least one optically active compound and/or at least one polymerizablecompound.
 31. The liquid crystal composition according to claim 21,further containing at least one antioxidant and/or at least oneultraviolet light absorber.
 32. A liquid crystal display device,comprising the liquid crystal composition according to claim 21.